Canonical Allele Identifier: CA2036663715
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939970739
gnomAD v4: 12-52814368-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814368T>C , CM000674.2:g.52814368T>C GRCh38
NC_000012.11:g.53208152T>C , CM000674.1:g.53208152T>C GRCh37
NC_000012.10:g.51494419T>C NCBI36
NG_007380.1:g.5184A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-310A>G ENSP00000448220.1:n.-310A>G
Search 100 bp 5'
Search 100 bp 3'