Canonical Allele Identifier: CA2036663704

Gene: KRT4

Linked Data

• dbSNP Id: rs1939970320
• gnomAD v4: 12-52814342-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814342C>T , CM000674.2:g.52814342C>T	GRCh38
NC_000012.11:g.53208126C>T , CM000674.1:g.53208126C>T	GRCh37
NC_000012.10:g.51494393C>T	NCBI36
NG_007380.1:g.5210G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-284G>A	ENSP00000448220.1:n.-284G>A