Canonical Allele Identifier: CA185510391

Gene:

Linked Data

• dbSNP Id: rs191977671
• gnomAD v2: 8-126486383-C-G
• gnomAD v3: 8-125474141-C-G
• gnomAD v4: 8-125474141-C-G
• MyVariant Identifiers: chr8:g.126486383C>G (hg19) ; chr8:g.125474141C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125474141C>G , CM000670.2:g.125474141C>G	GRCh38
NC_000008.10:g.126486383C>G , CM000670.1:g.126486383C>G	GRCh37
NC_000008.9:g.126555565C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+827C>G