Canonical Allele Identifier: CA255087088

Gene:

Linked Data

• dbSNP Id: rs778170880
• MyVariant Identifiers: chr13:g.95505183A>G (hg19) ; chr13:g.94852929A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.94852929A>G , CM000675.2:g.94852929A>G	GRCh38
NC_000013.10:g.95505183A>G , CM000675.1:g.95505183A>G	GRCh37
NC_000013.9:g.94303184A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110754.1:n.257-52535A>G