Canonical Allele Identifier: CA191701713
Gene:

Linked Data

dbSNP Id: rs183633600
gnomAD v2: 9-25551468-G-A
gnomAD v3: 9-25551470-G-A
gnomAD v4: 9-25551470-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551470G>A , CM000671.2:g.25551470G>A GRCh38
NC_000009.11:g.25551468G>A , CM000671.1:g.25551468G>A GRCh37
NC_000009.10:g.25541468G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-898C>T
XR_929525.2:n.674-898C>T