Canonical Allele Identifier: CA2726081042
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1342975250
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814339T>G , CM000674.2:g.52814339T>G GRCh38
NC_000012.11:g.53208123T>G , CM000674.1:g.53208123T>G GRCh37
NC_000012.10:g.51494390T>G NCBI36
NG_007380.1:g.5213A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-281A>C ENSP00000448220.1:n.-281A>C
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