Canonical Allele Identifier: CA742240584

Gene:

Linked Data

• dbSNP Id: rs1377031471
• MyVariant Identifiers: chr20:g.23642245A>G (hg19) ; chr20:g.23661608A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23661608A>G , CM000682.2:g.23661608A>G	GRCh38
NC_000020.10:g.23642245A>G , CM000682.1:g.23642245A>G	GRCh37
NC_000020.9:g.23590245A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001754712.1:n.238A>G