Canonical Allele Identifier: CA185510885

Gene:

Linked Data

• dbSNP Id: rs1037845352
• gnomAD v3: 8-125478493-C-G
• gnomAD v4: 8-125478493-C-G
• MyVariant Identifiers: chr8:g.126490735C>G (hg19) ; chr8:g.125478493C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478493C>G , CM000670.2:g.125478493C>G	GRCh38
NC_000008.10:g.126490735C>G , CM000670.1:g.126490735C>G	GRCh37
NC_000008.9:g.126559917C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5179C>G