Canonical Allele Identifier: CA2739419862
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814166T>G , CM000674.2:g.52814166T>G GRCh38
NC_000012.11:g.53207950T>G , CM000674.1:g.53207950T>G GRCh37
NC_000012.10:g.51494217T>G NCBI36
NG_007380.1:g.5386A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-108A>C ENSP00000448220.1:n.-108A>C