Canonical Allele Identifier: CA14920919
Gene: MAPK1 HGNC NCBI

Linked Data

dbSNP Id: rs6928
gnomAD v2: 22-22115004-C-G
gnomAD v3: 22-21760715-C-G
gnomAD v4: 22-21760715-C-G
MyVariant Identifiers: chr22:g.22115004C>G (hg19) chr22:g.21760715C>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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