Canonical Allele Identifier: CA715257071

Gene:

Linked Data

• dbSNP Id: rs1473912093
• gnomAD v3: 15-69755697-T-G
• gnomAD v4: 15-69755697-T-G
• MyVariant Identifiers: chr15:g.70048036T>G (hg19) ; chr15:g.69755697T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.69755697T>G , CM000677.2:g.69755697T>G	GRCh38
NC_000015.9:g.70048036T>G , CM000677.1:g.70048036T>G	GRCh37
NC_000015.8:g.67835090T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751592.2:n.86-459T>G