Canonical Allele Identifier: CA1033290845
Gene:

Linked Data

dbSNP Id: rs1672672225
gnomAD v3: 2-88016067-C-T
gnomAD v4: 2-88016067-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016067C>T , CM000664.2:g.88016067C>T GRCh38
NC_000002.11:g.88315586C>T , CM000664.1:g.88315586C>T GRCh37
NC_000002.10:g.88096701C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.412C>T
XR_940336.3:n.412C>T