Canonical Allele Identifier: CA304445755
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1194792
ClinVar RCV Id: RCV001557658
dbSNP Id: rs188271658
gnomAD v2: 19-4090834-C-T
gnomAD v3: 19-4090836-C-T
gnomAD v4: 19-4090836-C-T
MyVariant Identifiers: chr19:g.4090834C>T (hg19) chr19:g.4090836C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090836C>T , CM000681.2:g.4090836C>T GRCh38
NC_000019.9:g.4090834C>T , CM000681.1:g.4090834C>T GRCh37
NC_000019.8:g.4041834C>T NCBI36
NG_007996.1:g.38293G>A , LRG_750:g.38293G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-128G>A
ENST00000688002.1:n.3244-128G>A
ENST00000688751.1:n.229-128G>A
ENST00000689792.1:n.997-128G>A
ENST00000262948.10:c.1093-128G>A MANE Select ENSP00000262948.4:n.1093-128G>A
ENST00000262948.9:c.1093-128G>A ENSP00000262948.3:n.1093-128G>A
ENST00000394867.8:c.802-128G>A ENSP00000378336.1:n.802-128G>A
ENST00000597263.5:n.278-128G>A
ENST00000599021.1:c.203-128G>A
ENST00000600584.5:n.2542-128G>A
ENST00000601786.5:n.1394-128G>A
NM_030662.3:c.1093-128G>A , LRG_750t1:c.1093-128G>A NP_109587.1:n.1093-128G>A
XM_006722799.2:c.814-128G>A XP_006722862.1:n.814-128G>A
XM_011528133.1:c.523-128G>A XP_011526435.1:n.523-128G>A
NM_030662.4:c.1093-128G>A MANE Select NP_109587.1:n.1093-128G>A
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