Canonical Allele Identifier: CA2790193552
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444561C>A , CM000673.2:g.2444561C>A GRCh38
NC_000011.9:g.2465791C>A , CM000673.1:g.2465791C>A GRCh37
NC_000011.8:g.2422367C>A NCBI36
NG_008935.1:g.4571C>A , LRG_287:g.4571C>A

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.10G>T