Canonical Allele Identifier: CA11369388
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87734826A>G , CM000665.2:g.87734826A>G GRCh38
NC_000003.11:g.87783976A>G , CM000665.1:g.87783976A>G GRCh37
NC_000003.10:g.87866666A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941033.1:n.323-3076T>C
XR_941033.2:n.313-3076T>C