Canonical Allele Identifier: CA2036663661
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939968763

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814236C>A , CM000674.2:g.52814236C>A GRCh38
NC_000012.11:g.53208020C>A , CM000674.1:g.53208020C>A GRCh37
NC_000012.10:g.51494287C>A NCBI36
NG_007380.1:g.5316G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-178G>T ENSP00000448220.1:n.-178G>T