Canonical Allele Identifier: CA173376499
Gene:

Linked Data

dbSNP Id: rs530062138
gnomAD v2: 8-19987646-A-C
gnomAD v3: 8-20130135-A-C
gnomAD v4: 8-20130135-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130135A>C , CM000670.2:g.20130135A>C GRCh38
NC_000008.10:g.19987646A>C , CM000670.1:g.19987646A>C GRCh37
NC_000008.9:g.20031926A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949563.1:n.3408+216A>C
XR_949563.2:n.3400+216A>C