Canonical Allele Identifier: CA273056110

Gene:

Linked Data

• dbSNP Id: rs1046652726
• gnomAD v3: 15-69755753-G-A
• gnomAD v4: 15-69755753-G-A
• MyVariant Identifiers: chr15:g.70048092G>A (hg19) ; chr15:g.69755753G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.69755753G>A , CM000677.2:g.69755753G>A	GRCh38
NC_000015.9:g.70048092G>A , CM000677.1:g.70048092G>A	GRCh37
NC_000015.8:g.67835146G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001751592.2:n.86-403G>A