Canonical Allele Identifier: CA12179995
Gene:

Linked Data

dbSNP Id: rs6929568
gnomAD v2: 6-8228942-T-G
gnomAD v3: 6-8228709-T-G
gnomAD v4: 6-8228709-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8228709T>G , CM000668.2:g.8228709T>G GRCh38
NC_000006.11:g.8228942T>G , CM000668.1:g.8228942T>G GRCh37
NC_000006.10:g.8173941T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926440.1:n.83-1405T>G
XR_926441.1:n.190-10222T>G
XR_926442.1:n.83-1405T>G
XR_926443.1:n.83-10222T>G
XR_001743950.1:n.180-10222T>G
XR_926440.2:n.75-1405T>G
XR_926441.2:n.180-10222T>G
XR_926443.2:n.84-10222T>G