Canonical Allele Identifier: CA968854765

Gene:

Linked Data

• dbSNP Id: rs1894673381
• gnomAD v3: 15-38614849-C-A
• gnomAD v4: 15-38614849-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38614849C>A , CM000677.2:g.38614849C>A	GRCh38
NC_000015.9:g.38907050C>A , CM000677.1:g.38907050C>A	GRCh37
NC_000015.8:g.36694342C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751736.1:n.281+2394C>A