Canonical Allele Identifier: CA191701711
Gene:

Linked Data

dbSNP Id: rs899130308

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551465C>A , CM000671.2:g.25551465C>A GRCh38
NC_000009.11:g.25551463C>A , CM000671.1:g.25551463C>A GRCh37
NC_000009.10:g.25541463C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-893G>T
XR_929525.2:n.674-893G>T