Canonical Allele Identifier: CA2735341194
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs747851910
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090567C>T , CM000681.2:g.4090567C>T GRCh38
NC_000019.9:g.4090565C>T , CM000681.1:g.4090565C>T GRCh37
NC_000019.8:g.4041565C>T NCBI36
NG_007996.1:g.38562G>A , LRG_750:g.38562G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1673G>A
ENST00000688002.1:n.3385G>A
ENST00000688751.1:n.370G>A
ENST00000689792.1:n.1138G>A
ENST00000262948.10:c.*31G>A MANE Select ENSP00000262948.4:n.*31G>A
ENST00000262948.9:c.*31G>A ENSP00000262948.3:n.*31G>A
ENST00000394867.8:c.*31G>A ENSP00000378336.1:n.*31G>A
ENST00000597263.5:n.419G>A
ENST00000600584.5:n.2683G>A
ENST00000601786.5:n.1535G>A
NM_030662.3:c.*31G>A , LRG_750t1:c.*31G>A NP_109587.1:n.*31G>A
XM_006722799.2:c.*31G>A XP_006722862.1:n.*31G>A
XM_011528133.1:c.*31G>A XP_011526435.1:n.*31G>A
NM_030662.4:c.*31G>A MANE Select NP_109587.1:n.*31G>A
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