Canonical Allele Identifier: CA882241151
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1218920509
gnomAD v3: 19-4090325-C-A
gnomAD v4: 19-4090325-C-A
MyVariant Identifiers: chr19:g.4090323C>A (hg19) chr19:g.4090325C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090325C>A , CM000681.2:g.4090325C>A GRCh38
NC_000019.9:g.4090323C>A , CM000681.1:g.4090323C>A GRCh37
NC_000019.8:g.4041323C>A NCBI36
NG_007996.1:g.38804G>T , LRG_750:g.38804G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689792.1:n.1380G>T
ENST00000262948.10:c.*273G>T MANE Select ENSP00000262948.4:n.*273G>T
ENST00000262948.9:c.*273G>T ENSP00000262948.3:n.*273G>T
ENST00000600584.5:n.2925G>T
ENST00000601786.5:n.1777G>T
NM_030662.3:c.*273G>T , LRG_750t1:c.*273G>T NP_109587.1:n.*273G>T
XM_006722799.2:c.*273G>T XP_006722862.1:n.*273G>T
XM_011528133.1:c.*273G>T XP_011526435.1:n.*273G>T
NM_030662.4:c.*273G>T MANE Select NP_109587.1:n.*273G>T
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