Canonical Allele Identifier: CA2036663689
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs773268060

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814318C>A , CM000674.2:g.52814318C>A GRCh38
NC_000012.11:g.53208102C>A , CM000674.1:g.53208102C>A GRCh37
NC_000012.10:g.51494369C>A NCBI36
NG_007380.1:g.5234G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-260G>T ENSP00000448220.1:n.-260G>T