Canonical Allele Identifier: CA275015069

Gene:

Linked Data

• dbSNP Id: rs1046547453
• gnomAD v2: 15-87962511-A-G
• gnomAD v3: 15-87419280-A-G
• gnomAD v4: 15-87419280-A-G
• MyVariant Identifiers: chr15:g.87962511A>G (hg19) ; chr15:g.87419280A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419280A>G , CM000677.2:g.87419280A>G	GRCh38
NC_000015.9:g.87962511A>G , CM000677.1:g.87962511A>G	GRCh37
NC_000015.8:g.85763515A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-9T>C
XR_932585.1:n.340-9T>C
XR_001751647.1:n.617-9T>C
XR_932585.2:n.627-9T>C