Canonical Allele Identifier: CA2020573332
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20320824C>G , CM000674.2:g.20320824C>G GRCh38
NC_000012.11:g.20473758C>G , CM000674.1:g.20473758C>G GRCh37
NC_000012.10:g.20365025C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931419.1:n.154G>C
XR_931419.2:n.250G>C