Canonical Allele Identifier: CA862568165
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551376G>C , CM000671.2:g.25551376G>C GRCh38
NC_000009.11:g.25551374G>C , CM000671.1:g.25551374G>C GRCh37
NC_000009.10:g.25541374G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-804C>G
XR_929525.2:n.674-804C>G