Canonical Allele Identifier: CA715257140

Gene:

Linked Data

• dbSNP Id: rs1280736875
• gnomAD v3: 15-69755774-A-G
• gnomAD v4: 15-69755774-A-G
• MyVariant Identifiers: chr15:g.70048113A>G (hg19) ; chr15:g.69755774A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.69755774A>G , CM000677.2:g.69755774A>G	GRCh38
NC_000015.9:g.70048113A>G , CM000677.1:g.70048113A>G	GRCh37
NC_000015.8:g.67835167A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001751592.2:n.86-382A>G