Canonical Allele Identifier: CA2263926984

Gene:

Linked Data

• dbSNP Id: rs1908571163
• gnomAD v4: 17-50211857-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50211857C>T , CM000679.2:g.50211857C>T	GRCh38
NC_000017.10:g.48289218C>T , CM000679.1:g.48289218C>T	GRCh37
NC_000017.9:g.45644217C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934838.1:n.43-1978C>T