Canonical Allele Identifier: CA384946734
Gene: KRT2 HGNC NCBI

Linked Data

dbSNP Id: rs1941265079
MyVariant Identifiers: chr12:g.53045925A>G (hg19) chr12:g.52652141A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652141A>G , CM000674.2:g.52652141A>G GRCh38
NC_000012.11:g.53045925A>G , CM000674.1:g.53045925A>G GRCh37
NC_000012.10:g.51332192A>G NCBI36
NG_008296.1:g.5035T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.2T>C MANE Select ENSP00000310861.3:p.Met1Thr
ENST00000309680.3:c.2T>C ENSP00000310861.3:p.Met1Thr
NM_000423.2:c.2T>C NP_000414.2:p.Met1Thr
NM_000423.3:c.2T>C MANE Select NP_000414.2:p.Met1Thr
Search 100 bp 5'
Search 100 bp 3'