Canonical Allele Identifier: CA947716434
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939969099
gnomAD v3: 12-52814260-A-C
gnomAD v4: 12-52814260-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814260A>C , CM000674.2:g.52814260A>C GRCh38
NC_000012.11:g.53208044A>C , CM000674.1:g.53208044A>C GRCh37
NC_000012.10:g.51494311A>C NCBI36
NG_007380.1:g.5292T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-202T>G ENSP00000448220.1:n.-202T>G
Search 100 bp 5'
Search 100 bp 3'