Canonical Allele Identifier: CA2584876637
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1449764381
gnomAD v4: 19-4090558-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090558T>G , CM000681.2:g.4090558T>G GRCh38
NC_000019.9:g.4090556T>G , CM000681.1:g.4090556T>G GRCh37
NC_000019.8:g.4041556T>G NCBI36
NG_007996.1:g.38571A>C , LRG_750:g.38571A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1682A>C
ENST00000688002.1:n.3394A>C
ENST00000688751.1:n.379A>C
ENST00000689792.1:n.1147A>C
ENST00000262948.10:c.*40A>C MANE Select ENSP00000262948.4:n.*40A>C
ENST00000262948.9:c.*40A>C ENSP00000262948.3:n.*40A>C
ENST00000394867.8:c.*40A>C ENSP00000378336.1:n.*40A>C
ENST00000597263.5:n.428A>C
ENST00000600584.5:n.2692A>C
ENST00000601786.5:n.1544A>C
NM_030662.3:c.*40A>C , LRG_750t1:c.*40A>C NP_109587.1:n.*40A>C
XM_006722799.2:c.*40A>C XP_006722862.1:n.*40A>C
XM_011528133.1:c.*40A>C XP_011526435.1:n.*40A>C
NM_030662.4:c.*40A>C MANE Select NP_109587.1:n.*40A>C
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