Canonical Allele Identifier: CA275015083

Gene:

Linked Data

• dbSNP Id: rs189520367
• gnomAD v2: 15-87962596-G-C
• gnomAD v3: 15-87419365-G-C
• gnomAD v4: 15-87419365-G-C
• MyVariant Identifiers: chr15:g.87962596G>C (hg19) ; chr15:g.87419365G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419365G>C , CM000677.2:g.87419365G>C	GRCh38
NC_000015.9:g.87962596G>C , CM000677.1:g.87962596G>C	GRCh37
NC_000015.8:g.85763600G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-94C>G
XR_932585.1:n.340-94C>G
XR_001751647.1:n.617-94C>G
XR_932585.2:n.627-94C>G