Canonical Allele Identifier: CA269308942

Gene:

Linked Data

• dbSNP Id: rs778359229
• gnomAD v3: 15-38614857-C-T
• gnomAD v4: 15-38614857-C-T
• MyVariant Identifiers: chr15:g.38907058C>T (hg19) ; chr15:g.38614857C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38614857C>T , CM000677.2:g.38614857C>T	GRCh38
NC_000015.9:g.38907058C>T , CM000677.1:g.38907058C>T	GRCh37
NC_000015.8:g.36694350C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751736.1:n.281+2402C>T