Canonical Allele Identifier: CA1033291632
Gene:

Linked Data

dbSNP Id: rs367574790
gnomAD v3: 2-88016353-T-C
gnomAD v4: 2-88016353-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016353T>C , CM000664.2:g.88016353T>C GRCh38
NC_000002.11:g.88315872T>C , CM000664.1:g.88315872T>C GRCh37
NC_000002.10:g.88096987T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.698T>C
XR_940336.3:n.698T>C