Canonical Allele Identifier: CA464177715

Gene: CTAGE12P

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27610659A>C , CM000671.2:g.27610659A>C	GRCh38
NC_000009.11:g.27610657A>C , CM000671.1:g.27610657A>C	GRCh37
NC_000009.10:g.27600657A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400348.3:n.87T>G