Canonical Allele Identifier: CA1149684836
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2569899C>G , CM000663.2:g.2569899C>G GRCh38
NC_000001.10:g.2501338C>G , CM000663.1:g.2501338C>G GRCh37
NC_000001.9:g.2491198C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121638.1:n.71+3294C>G
XR_946834.1:n.1945C>G