Canonical Allele Identifier: CA1205765958

Gene:

Linked Data

• dbSNP Id: rs1648343091
• gnomAD v3: 1-168649280-C-A
• gnomAD v4: 1-168649280-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649280C>A , CM000663.2:g.168649280C>A	GRCh38
NC_000001.10:g.168618518C>A , CM000663.1:g.168618518C>A	GRCh37
NC_000001.9:g.166885142C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-8005G>T
XR_922259.2:n.332-8005G>T