Canonical Allele Identifier: CA973101898

Gene:

Linked Data

• dbSNP Id: rs1899530693
• gnomAD v3: 15-95782367-C-G
• gnomAD v4: 15-95782367-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.95782367C>G , CM000677.2:g.95782367C>G	GRCh38
NC_000015.9:g.96325596C>G , CM000677.1:g.96325596C>G	GRCh37
NC_000015.8:g.94126600C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932654.1:n.148-42822C>G