Canonical Allele Identifier: CA619725783

Gene:

Linked Data

• dbSNP Id: rs1338979851
• gnomAD v2: 15-87695443-T-A
• gnomAD v3: 15-87152212-T-A
• gnomAD v4: 15-87152212-T-A
• MyVariant Identifiers: chr15:g.87695443T>A (hg19) ; chr15:g.87152212T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87152212T>A , CM000677.2:g.87152212T>A	GRCh38
NC_000015.9:g.87695443T>A , CM000677.1:g.87695443T>A	GRCh37
NC_000015.8:g.85496447T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932582.1:n.167-26015T>A
XR_932582.2:n.167-26015T>A