Canonical Allele Identifier: CA617508899

Gene:

Linked Data

• dbSNP Id: rs1443541126
• gnomAD v2: 15-38907093-G-A
• gnomAD v3: 15-38614892-G-A
• gnomAD v4: 15-38614892-G-A
• MyVariant Identifiers: chr15:g.38907093G>A (hg19) ; chr15:g.38614892G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38614892G>A , CM000677.2:g.38614892G>A	GRCh38
NC_000015.9:g.38907093G>A , CM000677.1:g.38907093G>A	GRCh37
NC_000015.8:g.36694385G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751736.1:n.281+2437G>A