Canonical Allele Identifier: CA634913693

Gene:

Linked Data

• dbSNP Id: rs1335210121
• gnomAD v2: 20-23642486-A-G
• gnomAD v3: 20-23661849-A-G
• gnomAD v4: 20-23661849-A-G
• MyVariant Identifiers: chr20:g.23642486A>G (hg19) ; chr20:g.23661849A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23661849A>G , CM000682.2:g.23661849A>G	GRCh38
NC_000020.10:g.23642486A>G , CM000682.1:g.23642486A>G	GRCh37
NC_000020.9:g.23590486A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001754712.1:n.280+199A>G