Canonical Allele Identifier: CA2590630312
Gene:

Linked Data

dbSNP Id: rs151198311
gnomAD v3: 6-465983-T-G
gnomAD v4: 6-465983-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465983T>G , CM000668.2:g.465983T>G GRCh38
NC_000006.11:g.465983T>G , CM000668.1:g.465983T>G GRCh37
NC_000006.10:g.410983T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12258T>G
XR_926365.1:n.2548+12258T>G
XR_001743914.1:n.482-9225T>G