Canonical Allele Identifier: CA605088153

Gene: KRT4

Linked Data

• dbSNP Id: rs1407034676
• gnomAD v2: 12-53207984-A-C
• gnomAD v3: 12-52814200-A-C
• gnomAD v4: 12-52814200-A-C
• MyVariant Identifiers: chr12:g.53207984A>C (hg19) ; chr12:g.52814200A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814200A>C , CM000674.2:g.52814200A>C	GRCh38
NC_000012.11:g.53207984A>C , CM000674.1:g.53207984A>C	GRCh37
NC_000012.10:g.51494251A>C	NCBI36
NG_007380.1:g.5352T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-142T>G	ENSP00000448220.1:n.-142T>G