Canonical Allele Identifier: CA2263926969

Gene:

Linked Data

• dbSNP Id: rs1908570608
• gnomAD v4: 17-50211821-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50211821G>A , CM000679.2:g.50211821G>A	GRCh38
NC_000017.10:g.48289182G>A , CM000679.1:g.48289182G>A	GRCh37
NC_000017.9:g.45644181G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934838.1:n.43-2014G>A