Canonical Allele Identifier: CA1085192519
Gene:

Linked Data

dbSNP Id: rs1762568756
gnomAD v3: 6-465888-A-G
gnomAD v4: 6-465888-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465888A>G , CM000668.2:g.465888A>G GRCh38
NC_000006.11:g.465888A>G , CM000668.1:g.465888A>G GRCh37
NC_000006.10:g.410888A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12163A>G
XR_926365.1:n.2548+12163A>G
XR_001743914.1:n.482-9320A>G