Canonical Allele Identifier: CA742240587

Gene:

Linked Data

• dbSNP Id: rs1302392992
• MyVariant Identifiers: chr20:g.23642246C>T (hg19) ; chr20:g.23661609C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23661609C>T , CM000682.2:g.23661609C>T	GRCh38
NC_000020.10:g.23642246C>T , CM000682.1:g.23642246C>T	GRCh37
NC_000020.9:g.23590246C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001754712.1:n.239C>T