Canonical Allele Identifier: CA6588931

Gene: KRT4

Linked Data

• dbSNP Id: rs771161862
• ExAC: 12:53208105 T / C
• gnomAD v2: 12-53208105-T-C
• gnomAD v4: 12-52814321-T-C
• MyVariant Identifiers: chr12:g.53208105T>C (hg19) ; chr12:g.52814321T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814321T>C , CM000674.2:g.52814321T>C	GRCh38
NC_000012.11:g.53208105T>C , CM000674.1:g.53208105T>C	GRCh37
NC_000012.10:g.51494372T>C	NCBI36
NG_007380.1:g.5231A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-263A>G	ENSP00000448220.1:n.-263A>G