Canonical Allele Identifier: CA202788788

Gene:

Linked Data

• dbSNP Id: rs184314955
• MyVariant Identifiers: chr10:g.8739582T>C (hg19) ; chr10:g.8697619T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697619T>C , CM000672.2:g.8697619T>C	GRCh38
NC_000010.10:g.8739582T>C , CM000672.1:g.8739582T>C	GRCh37
NC_000010.9:g.8779588T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27818A>G