Canonical Allele Identifier: CA2773802985
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668568G>T , CM000668.2:g.160668568G>T GRCh38
NC_000006.11:g.161089600G>T , CM000668.1:g.161089600G>T GRCh37
NC_000006.10:g.161009590G>T NCBI36
NG_016147.1:g.2808C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2195C>A