Canonical Allele Identifier: CA276104119

Gene:

Linked Data

• dbSNP Id: rs556536492
• gnomAD v3: 15-95782342-A-T
• gnomAD v4: 15-95782342-A-T
• MyVariant Identifiers: chr15:g.96325571A>T (hg19) ; chr15:g.95782342A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.95782342A>T , CM000677.2:g.95782342A>T	GRCh38
NC_000015.9:g.96325571A>T , CM000677.1:g.96325571A>T	GRCh37
NC_000015.8:g.94126575A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932654.1:n.148-42847A>T