Canonical Allele Identifier: CA2551572112
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12108913T>C , CM000671.2:g.12108913T>C GRCh38
NC_000009.11:g.12108913T>C , CM000671.1:g.12108913T>C GRCh37
NC_000009.10:g.12098913T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929481.1:n.166+7908A>G
XR_929482.1:n.260+7908A>G
XR_929481.2:n.166+7908A>G
XR_929482.2:n.260+7908A>G