Canonical Allele Identifier: CA15658980
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94991513T>C , CM000672.2:g.94991513T>C GRCh38
NC_000010.10:g.96751270T>C , CM000672.1:g.96751270T>C GRCh37
NC_000010.9:g.96741260T>C NCBI36
NG_008385.2:g.58356T>C

Transcript Alleles

HGVS Amino-acid Change
XR_001747556.1:n.2949A>G