Canonical Allele Identifier: CA2036663641
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1565686073

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814179A>G , CM000674.2:g.52814179A>G GRCh38
NC_000012.11:g.53207963A>G , CM000674.1:g.53207963A>G GRCh37
NC_000012.10:g.51494230A>G NCBI36
NG_007380.1:g.5373T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-121T>C ENSP00000448220.1:n.-121T>C