Canonical Allele Identifier: CA947716459
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939970816

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814373G>A , CM000674.2:g.52814373G>A GRCh38
NC_000012.11:g.53208157G>A , CM000674.1:g.53208157G>A GRCh37
NC_000012.10:g.51494424G>A NCBI36
NG_007380.1:g.5179C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-315C>T ENSP00000448220.1:n.-315C>T