Canonical Allele Identifier: CA12934160

Gene:

Linked Data

• dbSNP Id: rs1963982
• gnomAD v2: 8-73106916-A-G
• gnomAD v3: 8-72194681-A-G
• gnomAD v4: 8-72194681-A-G
• MyVariant Identifiers: chr8:g.73106916A>G (hg19) ; chr8:g.72194681A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72194681A>G , CM000670.2:g.72194681A>G	GRCh38
NC_000008.10:g.73106916A>G , CM000670.1:g.73106916A>G	GRCh37
NC_000008.9:g.73269470A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929040.1:n.472A>G
XR_929040.2:n.1097A>G