Canonical Allele Identifier: CA2036663729
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939971206
gnomAD v4: 12-52814407-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814407T>A , CM000674.2:g.52814407T>A GRCh38
NC_000012.11:g.53208191T>A , CM000674.1:g.53208191T>A GRCh37
NC_000012.10:g.51494458T>A NCBI36
NG_007380.1:g.5145A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-349A>T ENSP00000448220.1:n.-349A>T
Search 100 bp 5'
Search 100 bp 3'