Canonical Allele Identifier: CA947716451
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939970042
gnomAD v3: 12-52814323-G-A
gnomAD v4: 12-52814323-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814323G>A , CM000674.2:g.52814323G>A GRCh38
NC_000012.11:g.53208107G>A , CM000674.1:g.53208107G>A GRCh37
NC_000012.10:g.51494374G>A NCBI36
NG_007380.1:g.5229C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-265C>T ENSP00000448220.1:n.-265C>T
Search 100 bp 5'
Search 100 bp 3'