Canonical Allele Identifier: CA717349450

Gene:

Linked Data

• dbSNP Id: rs1336146288
• gnomAD v3: 15-94775277-A-T
• gnomAD v4: 15-94775277-A-T
• MyVariant Identifiers: chr15:g.95318506A>T (hg19) ; chr15:g.94775277A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.94775277A>T , CM000677.2:g.94775277A>T	GRCh38
NC_000015.9:g.95318506A>T , CM000677.1:g.95318506A>T	GRCh37
NC_000015.8:g.93119510A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_932644.1:n.369-9260T>A
XR_932644.2:n.369-9260T>A