Canonical Allele Identifier: CA2507760673
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756023T>C , CM000671.2:g.21756023T>C GRCh38
NC_000009.11:g.21756022T>C , CM000671.1:g.21756022T>C GRCh37
NC_000009.10:g.21746022T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11802A>G