Canonical Allele Identifier: CA2036663732
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939971279

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814408C>G , CM000674.2:g.52814408C>G GRCh38
NC_000012.11:g.53208192C>G , CM000674.1:g.53208192C>G GRCh37
NC_000012.10:g.51494459C>G NCBI36
NG_007380.1:g.5144G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-350G>C ENSP00000448220.1:n.-350G>C