Canonical Allele Identifier: CA269308943

Gene:

Linked Data

• dbSNP Id: rs958709931
• MyVariant Identifiers: chr15:g.38907071A>G (hg19) ; chr15:g.38614870A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38614870A>G , CM000677.2:g.38614870A>G	GRCh38
NC_000015.9:g.38907071A>G , CM000677.1:g.38907071A>G	GRCh37
NC_000015.8:g.36694363A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751736.1:n.281+2415A>G