Canonical Allele Identifier: CA1098302699
Gene:

Linked Data

dbSNP Id: rs1305136385
gnomAD v3: 7-9816755-A-G
gnomAD v4: 7-9816755-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.9816755A>G , CM000669.2:g.9816755A>G GRCh38
NC_000007.13:g.9856384A>G , CM000669.1:g.9856384A>G GRCh37
NC_000007.12:g.9822909A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927024.1:n.209+50035T>C
XR_927025.1:n.323+50035T>C
XR_927026.1:n.209+50035T>C
XR_927026.2:n.209+50035T>C