Canonical Allele Identifier: CA6588897

Gene: KRT4

Linked Data

• dbSNP Id: rs762487825
• ExAC: 12:53207932 TC / T
• gnomAD v2: 12-53207932-TC-T
• MyVariant Identifiers: chr12:g.53207933del (hg19) ; chr12:g.52814149del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814150del , CM000674.2:g.52814150del	GRCh38
NC_000012.11:g.53207934del , CM000674.1:g.53207934del	GRCh37
NC_000012.10:g.51494201del	NCBI36
NG_007380.1:g.5403del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-91del	ENSP00000448220.1:n.-91del