Canonical Allele Identifier: CA269308947

Gene:

Linked Data

• dbSNP Id: rs112426395
• gnomAD v3: 15-38614879-A-G
• gnomAD v4: 15-38614879-A-G
• MyVariant Identifiers: chr15:g.38907080A>G (hg19) ; chr15:g.38614879A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38614879A>G , CM000677.2:g.38614879A>G	GRCh38
NC_000015.9:g.38907080A>G , CM000677.1:g.38907080A>G	GRCh37
NC_000015.8:g.36694372A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751736.1:n.281+2424A>G