Canonical Allele Identifier: CA1419898220
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170412314C>G , CM000665.2:g.170412314C>G GRCh38
NC_000003.11:g.170130102C>G , CM000665.1:g.170130102C>G GRCh37
NC_000003.10:g.171612796C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924700.1:n.238-483C>G