Canonical Allele Identifier: CA103340613
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.104923116T>G , CM000666.2:g.104923116T>G GRCh38
NC_000004.11:g.105844273T>G , CM000666.1:g.105844273T>G GRCh37
NC_000004.10:g.106063722T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939034.1:n.79-495T>G
XR_939035.1:n.79-495T>G