Canonical Allele Identifier: CA725798568

Gene:

Linked Data

• dbSNP Id: rs1316795132
• MyVariant Identifiers: chr16:g.9343564C>G (hg19) ; chr16:g.9249707C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249707C>G , CM000678.2:g.9249707C>G	GRCh38
NC_000016.9:g.9343564C>G , CM000678.1:g.9343564C>G	GRCh37
NC_000016.8:g.9251065C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64974C>G