Canonical Allele Identifier: CA2509287786
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668463T>A , CM000668.2:g.160668463T>A GRCh38
NC_000006.11:g.161089495T>A , CM000668.1:g.161089495T>A GRCh37
NC_000006.10:g.161009485T>A NCBI36
NG_016147.1:g.2913A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2090A>T