Canonical Allele Identifier: CA273056108

Gene:

Linked Data

• dbSNP Id: rs762837568
• gnomAD v3: 15-69755745-C-G
• gnomAD v4: 15-69755745-C-G
• MyVariant Identifiers: chr15:g.70048084C>G (hg19) ; chr15:g.69755745C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.69755745C>G , CM000677.2:g.69755745C>G	GRCh38
NC_000015.9:g.70048084C>G , CM000677.1:g.70048084C>G	GRCh37
NC_000015.8:g.67835138C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001751592.2:n.86-411C>G