Canonical Allele Identifier: CA181599862

Gene:

Linked Data

• dbSNP Id: rs901054525
• gnomAD v3: 8-88981062-C-G
• gnomAD v4: 8-88981062-C-G
• MyVariant Identifiers: chr8:g.89993291C>G (hg19) ; chr8:g.88981062C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88981062C>G , CM000670.2:g.88981062C>G	GRCh38
NC_000008.10:g.89993291C>G , CM000670.1:g.89993291C>G	GRCh37
NC_000008.9:g.90062407C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002956667.1:n.179-99001G>C