Canonical Allele Identifier: CA153770485
Gene:

Linked Data

dbSNP Id: rs117749535
gnomAD v2: 7-9856508-A-G
gnomAD v3: 7-9816879-A-G
gnomAD v4: 7-9816879-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.9816879A>G , CM000669.2:g.9816879A>G GRCh38
NC_000007.13:g.9856508A>G , CM000669.1:g.9856508A>G GRCh37
NC_000007.12:g.9823033A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927024.1:n.209+49911T>C
XR_927025.1:n.323+49911T>C
XR_927026.1:n.209+49911T>C
XR_927026.2:n.209+49911T>C