Canonical Allele Identifier: CA583781689

Gene:

Linked Data

• dbSNP Id: rs1410378489
• gnomAD v2: 8-98281682-C-T
• gnomAD v3: 8-97269454-C-T
• gnomAD v4: 8-97269454-C-T
• MyVariant Identifiers: chr8:g.98281682C>T (hg19) ; chr8:g.97269454C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269454C>T , CM000670.2:g.97269454C>T	GRCh38
NC_000008.10:g.98281682C>T , CM000670.1:g.98281682C>T	GRCh37
NC_000008.9:g.98350858C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125390.1:n.471+149616G>A