Canonical Allele Identifier: CA2552557064
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756031A>G , CM000671.2:g.21756031A>G GRCh38
NC_000009.11:g.21756030A>G , CM000671.1:g.21756030A>G GRCh37
NC_000009.10:g.21746030A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746563.2:n.163+11794T>C