Canonical Allele Identifier: CA6588902
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs777525045
ExAC: 12:53207946 G / A
gnomAD v2: 12-53207946-G-A
gnomAD v4: 12-52814162-G-A
MyVariant Identifiers: chr12:g.53207946G>A (hg19) chr12:g.52814162G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814162G>A , CM000674.2:g.52814162G>A GRCh38
NC_000012.11:g.53207946G>A , CM000674.1:g.53207946G>A GRCh37
NC_000012.10:g.51494213G>A NCBI36
NG_007380.1:g.5390C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-104C>T ENSP00000448220.1:n.-104C>T
Search 100 bp 5'
Search 100 bp 3'