Canonical Allele Identifier: CA859577233
Gene:

Linked Data

dbSNP Id: rs1397330526

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12108948C>A , CM000671.2:g.12108948C>A GRCh38
NC_000009.11:g.12108948C>A , CM000671.1:g.12108948C>A GRCh37
NC_000009.10:g.12098948C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929481.1:n.166+7873G>T
XR_929482.1:n.260+7873G>T
XR_929481.2:n.166+7873G>T
XR_929482.2:n.260+7873G>T