Canonical Allele Identifier: CA2753078342
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260486C>G , CM000664.2:g.168260486C>G GRCh38
NC_000002.11:g.169116996C>G , CM000664.1:g.169116996C>G GRCh37
NC_000002.10:g.168825242C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739763.1:n.912-4610C>G
XR_001739764.1:n.318-4610C>G
XR_001739765.1:n.436-4610C>G