Canonical Allele Identifier: CA1008923848

Gene:

Linked Data

• dbSNP Id: rs1648342707
• gnomAD v3: 1-168649261-A-G
• gnomAD v4: 1-168649261-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649261A>G , CM000663.2:g.168649261A>G	GRCh38
NC_000001.10:g.168618499A>G , CM000663.1:g.168618499A>G	GRCh37
NC_000001.9:g.166885123A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-7986T>C
XR_922259.2:n.332-7986T>C