Canonical Allele Identifier: CA9090690
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525536
ClinVar RCV Id: RCV002036760 RCV003481257
dbSNP Id: rs565860695
ExAC: 19:4090658 C / T
gnomAD v2: 19-4090658-C-T
gnomAD v3: 19-4090660-C-T
gnomAD v4: 19-4090660-C-T
MyVariant Identifiers: chr19:g.4090658C>T (hg19) chr19:g.4090660C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090660C>T , CM000681.2:g.4090660C>T GRCh38
NC_000019.9:g.4090658C>T , CM000681.1:g.4090658C>T GRCh37
NC_000019.8:g.4041658C>T NCBI36
NG_007996.1:g.38469G>A , LRG_750:g.38469G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1580G>A
ENST00000688002.1:n.3292G>A
ENST00000688751.1:n.277G>A
ENST00000689792.1:n.1045G>A
ENST00000262948.10:c.1141G>A MANE Select ENSP00000262948.4:p.Gly381Ser
ENST00000262948.9:c.1141G>A ENSP00000262948.3:p.Gly381Ser
ENST00000394867.8:c.850G>A ENSP00000378336.1:p.Gly284Ser
ENST00000597263.5:n.326G>A
ENST00000599021.1:c.251G>A
ENST00000600584.5:n.2590G>A
ENST00000601786.5:n.1442G>A
NM_030662.3:c.1141G>A , LRG_750t1:c.1141G>A NP_109587.1:p.Gly381Ser
XM_006722799.2:c.862G>A XP_006722862.1:p.Gly288Ser
XM_011528133.1:c.571G>A XP_011526435.1:p.Gly191Ser
NM_030662.4:c.1141G>A MANE Select NP_109587.1:p.Gly381Ser
Search 100 bp 5'
Search 100 bp 3'