Canonical Allele Identifier: CA464177716

Gene: CTAGE12P

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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