Canonical Allele Identifier: CA384946047
Gene: KRT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53045863A>T (hg19) chr12:g.52652079A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652079A>T , CM000674.2:g.52652079A>T GRCh38
NC_000012.11:g.53045863A>T , CM000674.1:g.53045863A>T GRCh37
NC_000012.10:g.51332130A>T NCBI36
NG_008296.1:g.5097T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.64T>A MANE Select ENSP00000310861.3:p.Phe22Ile
ENST00000309680.3:c.64T>A ENSP00000310861.3:p.Phe22Ile
NM_000423.2:c.64T>A NP_000414.2:p.Phe22Ile
NM_000423.3:c.64T>A MANE Select NP_000414.2:p.Phe22Ile
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