Canonical Allele Identifier: CA882241159
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1421020698
gnomAD v3: 19-4090389-G-T
gnomAD v4: 19-4090389-G-T
MyVariant Identifiers: chr19:g.4090387G>T (hg19) chr19:g.4090389G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090389G>T , CM000681.2:g.4090389G>T GRCh38
NC_000019.9:g.4090387G>T , CM000681.1:g.4090387G>T GRCh37
NC_000019.8:g.4041387G>T NCBI36
NG_007996.1:g.38740C>A , LRG_750:g.38740C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1851C>A
ENST00000688751.1:n.548C>A
ENST00000689792.1:n.1316C>A
ENST00000262948.10:c.*209C>A MANE Select ENSP00000262948.4:n.*209C>A
ENST00000262948.9:c.*209C>A ENSP00000262948.3:n.*209C>A
ENST00000394867.8:c.*209C>A ENSP00000378336.1:n.*209C>A
ENST00000600584.5:n.2861C>A
ENST00000601786.5:n.1713C>A
NM_030662.3:c.*209C>A , LRG_750t1:c.*209C>A NP_109587.1:n.*209C>A
XM_006722799.2:c.*209C>A XP_006722862.1:n.*209C>A
XM_011528133.1:c.*209C>A XP_011526435.1:n.*209C>A
NM_030662.4:c.*209C>A MANE Select NP_109587.1:n.*209C>A
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