Canonical Allele Identifier: CA882241179
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1173256435
MyVariant Identifiers: chr19:g.4090457G>A (hg19) chr19:g.4090459G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090459G>A , CM000681.2:g.4090459G>A GRCh38
NC_000019.9:g.4090457G>A , CM000681.1:g.4090457G>A GRCh37
NC_000019.8:g.4041457G>A NCBI36
NG_007996.1:g.38670C>T , LRG_750:g.38670C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1781C>T
ENST00000688751.1:n.478C>T
ENST00000689792.1:n.1246C>T
ENST00000262948.10:c.*139C>T MANE Select ENSP00000262948.4:n.*139C>T
ENST00000262948.9:c.*139C>T ENSP00000262948.3:n.*139C>T
ENST00000394867.8:c.*139C>T ENSP00000378336.1:n.*139C>T
ENST00000597263.5:n.527C>T
ENST00000600584.5:n.2791C>T
ENST00000601786.5:n.1643C>T
NM_030662.3:c.*139C>T , LRG_750t1:c.*139C>T NP_109587.1:n.*139C>T
XM_006722799.2:c.*139C>T XP_006722862.1:n.*139C>T
XM_011528133.1:c.*139C>T XP_011526435.1:n.*139C>T
NM_030662.4:c.*139C>T MANE Select NP_109587.1:n.*139C>T
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