Canonical Allele Identifier: CA631537151
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1249048457
gnomAD v2: 19-4090709-G-T
gnomAD v4: 19-4090711-G-T
MyVariant Identifiers: chr19:g.4090709G>T (hg19) chr19:g.4090711G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090711G>T , CM000681.2:g.4090711G>T GRCh38
NC_000019.9:g.4090709G>T , CM000681.1:g.4090709G>T GRCh37
NC_000019.8:g.4041709G>T NCBI36
NG_007996.1:g.38418C>A , LRG_750:g.38418C>A

Transcript Alleles

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