Canonical Allele Identifier: CA275015087

Gene:

Linked Data

• dbSNP Id: rs748496998
• gnomAD v2: 15-87962606-T-C
• gnomAD v3: 15-87419375-T-C
• gnomAD v4: 15-87419375-T-C
• MyVariant Identifiers: chr15:g.87962606T>C (hg19) ; chr15:g.87419375T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419375T>C , CM000677.2:g.87419375T>C	GRCh38
NC_000015.9:g.87962606T>C , CM000677.1:g.87962606T>C	GRCh37
NC_000015.8:g.85763610T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-104A>G
XR_932585.1:n.340-104A>G
XR_001751647.1:n.617-104A>G
XR_932585.2:n.627-104A>G