Canonical Allele Identifier: CA313629857

Gene:

Linked Data

• dbSNP Id: rs896375144
• MyVariant Identifiers: chr20:g.23642505A>T (hg19) ; chr20:g.23661868A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23661868A>T , CM000682.2:g.23661868A>T	GRCh38
NC_000020.10:g.23642505A>T , CM000682.1:g.23642505A>T	GRCh37
NC_000020.9:g.23590505A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001754712.1:n.280+218A>T