Canonical Allele Identifier: CA2036663712
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939970663
gnomAD v4: 12-52814366-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814366C>A , CM000674.2:g.52814366C>A GRCh38
NC_000012.11:g.53208150C>A , CM000674.1:g.53208150C>A GRCh37
NC_000012.10:g.51494417C>A NCBI36
NG_007380.1:g.5186G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-308G>T ENSP00000448220.1:n.-308G>T
Search 100 bp 5'
Search 100 bp 3'