Canonical Allele Identifier: CA913427889

Gene:

Linked Data

• dbSNP Id: rs1564340125
• gnomAD v2: 10-8739534-G-C
• gnomAD v3: 10-8697571-G-C
• gnomAD v4: 10-8697571-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697571G>C , CM000672.2:g.8697571G>C	GRCh38
NC_000010.10:g.8739534G>C , CM000672.1:g.8739534G>C	GRCh37
NC_000010.9:g.8779540G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27770C>G