Canonical Allele Identifier: CA828661956

Gene:

Linked Data

• dbSNP Id: rs1277075124
• gnomAD v3: 6-8169778-G-T
• gnomAD v4: 6-8169778-G-T
• MyVariant Identifiers: chr6:g.8170011G>T (hg19) ; chr6:g.8169778G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.8169778G>T , CM000668.2:g.8169778G>T	GRCh38
NC_000006.11:g.8170011G>T , CM000668.1:g.8170011G>T	GRCh37
NC_000006.10:g.8115010G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926440.1:n.82+11518G>T
XR_926441.1:n.189+1858G>T
XR_926442.1:n.82+11518G>T
XR_926443.1:n.82+11518G>T
XR_001743950.1:n.179+1858G>T
XR_926440.2:n.74+11518G>T
XR_926441.2:n.179+1858G>T
XR_926443.2:n.83+11518G>T