Canonical Allele Identifier: CA275015075

Gene:

Linked Data

• dbSNP Id: rs376925797
• gnomAD v2: 15-87962539-G-T
• gnomAD v3: 15-87419308-G-T
• gnomAD v4: 15-87419308-G-T
• MyVariant Identifiers: chr15:g.87962539G>T (hg19) ; chr15:g.87419308G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419308G>T , CM000677.2:g.87419308G>T	GRCh38
NC_000015.9:g.87962539G>T , CM000677.1:g.87962539G>T	GRCh37
NC_000015.8:g.85763543G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-37C>A
XR_932585.1:n.340-37C>A
XR_001751647.1:n.617-37C>A
XR_932585.2:n.627-37C>A