Canonical Allele Identifier: CA2043863984
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68247752T>G , CM000674.2:g.68247752T>G GRCh38
NC_000012.11:g.68641532T>G , CM000674.1:g.68641532T>G GRCh37
NC_000012.10:g.66927799T>G NCBI36
NG_060763.1:g.10853A>C

Transcript Alleles

HGVS Amino-acid Change
XR_945055.1:n.265-16906T>G
XR_002957418.1:n.281-16906T>G