Canonical Allele Identifier: CA2726183708
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs2121258791

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814252A>C , CM000674.2:g.52814252A>C GRCh38
NC_000012.11:g.53208036A>C , CM000674.1:g.53208036A>C GRCh37
NC_000012.10:g.51494303A>C NCBI36
NG_007380.1:g.5300T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-194T>G ENSP00000448220.1:n.-194T>G