Canonical Allele Identifier: CA1842217827
Gene: CTAGE12P HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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