Canonical Allele Identifier: CA1619879878
Gene:

Linked Data

dbSNP Id: rs2294478
gnomAD v4: 6-33131189-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33131189C>G , CM000668.2:g.33131189C>G GRCh38
NC_000006.11:g.33098966C>G , CM000668.1:g.33098966C>G GRCh37
NC_000006.10:g.33206944C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926703.1:n.670-90G>C
XR_001744086.1:n.831+8G>C
XR_926703.2:n.680-90G>C