Canonical Allele Identifier: CA1104780584
Gene:

Linked Data

dbSNP Id: rs1789256157
gnomAD v3: 7-97388348-A-G
gnomAD v4: 7-97388348-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388348A>G , CM000669.2:g.97388348A>G GRCh38
NC_000007.13:g.97017660A>G , CM000669.1:g.97017660A>G GRCh37
NC_000007.12:g.96855596A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59701T>C