Canonical Allele Identifier: CA1008923904

Gene:

Linked Data

• dbSNP Id: rs959832108
• gnomAD v3: 1-168649537-C-T
• gnomAD v4: 1-168649537-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649537C>T , CM000663.2:g.168649537C>T	GRCh38
NC_000001.10:g.168618775C>T , CM000663.1:g.168618775C>T	GRCh37
NC_000001.9:g.166885399C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-8262G>A
XR_922259.2:n.332-8262G>A