Canonical Allele Identifier: CA587286385
Gene:

Linked Data

dbSNP Id: rs1463984833
gnomAD v2: 9-25551473-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551475G>A , CM000671.2:g.25551475G>A GRCh38
NC_000009.11:g.25551473G>A , CM000671.1:g.25551473G>A GRCh37
NC_000009.10:g.25541473G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-903C>T
XR_929525.2:n.674-903C>T