Canonical Allele Identifier: CA2036663736
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939971446
gnomAD v4: 12-52814413-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814413T>G , CM000674.2:g.52814413T>G GRCh38
NC_000012.11:g.53208197T>G , CM000674.1:g.53208197T>G GRCh37
NC_000012.10:g.51494464T>G NCBI36
NG_007380.1:g.5139A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-355A>C ENSP00000448220.1:n.-355A>C
Search 100 bp 5'
Search 100 bp 3'