Canonical Allele Identifier: CA820836189

Gene:

Linked Data

• dbSNP Id: rs1462870042
• gnomAD v3: 6-151627157-A-G
• gnomAD v4: 6-151627157-A-G
• MyVariant Identifiers: chr6:g.151948292A>G (hg19) ; chr6:g.151627157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151627157A>G , CM000668.2:g.151627157A>G	GRCh38
NC_000006.11:g.151948292A>G , CM000668.1:g.151948292A>G	GRCh37
NC_000006.10:g.151989985A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943113.1:n.583A>G
XR_943115.1:n.583A>G