Canonical Allele Identifier: CA1139772263
Gene: MAPK1 HGNC NCBI

Linked Data

dbSNP Id: rs6928
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21760715C>A , CM000684.2:g.21760715C>A GRCh38
NC_000022.10:g.22115004C>A , CM000684.1:g.22115004C>A GRCh37
NC_000022.9:g.20445004C>A NCBI36
NG_023054.2:g.111966G>T , LRG_786:g.111966G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000215832.11:c.*3535G>T MANE Select ENSP00000215832.7:n.*3535G>T
ENST00000215832.10:c.*3535G>T ENSP00000215832.6:n.*3535G>T
NM_002745.4:c.*3535G>T , LRG_786t1:c.*3535G>T NP_002736.3:n.*3535G>T
NM_002745.5:c.*3535G>T MANE Select NP_002736.3:n.*3535G>T
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