Canonical Allele Identifier: CA2036663633
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814167G= , CM000674.2:g.52814167G= GRCh38
NC_000012.11:g.53207951G= , CM000674.1:g.53207951G= GRCh37
NC_000012.10:g.51494218G= NCBI36
NG_007380.1:g.5385C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-109C= ENSP00000448220.1:n.-109C=