Linked Data
dbSNP Id:
rs890985819
gnomAD v3:
12-1719313-G-T
gnomAD v4:
12-1719313-G-T
MyVariant Identifiers:
chr12:g.1719313G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.1719313G>T , CM000674.2:g.1719313G>T | GRCh38 |
| NC_000012.11:g.1828479G>T , CM000674.1:g.1828479G>T | GRCh37 |
| NC_000012.10:g.1698740G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357103.5:c.-87+28122G>T MANE Select | ENSP00000349616.4:n.-87+28122G>T | |
| ENST00000357103.4:c.-87+28122G>T | ENSP00000349616.4:n.-87+28122G>T | |
| ENST00000537545.1:n.144+30596G>T | ||
| ENST00000540974.1:n.149-11412G>T | ||
| NM_024551.2:c.-87+28122G>T | NP_078827.2:n.-87+28122G>T | |
| XM_005253789.1:c.-87+28100G>T | XP_005253846.1:n.-87+28100G>T | |
| XM_006719018.1:c.-87+16331G>T | XP_006719081.1:n.-87+16331G>T | |
| XM_011521024.1:c.-87+16331G>T | XP_011519326.1:n.-87+16331G>T | |
| XM_011521025.1:c.-87+28100G>T | XP_011519327.1:n.-87+28100G>T | |
| XM_005253789.2:c.-87+28100G>T | XP_005253846.1:n.-87+28100G>T | |
| XM_006719018.2:c.-87+16331G>T | XP_006719081.1:n.-87+16331G>T | |
| XM_011521024.2:c.-87+16331G>T | XP_011519326.1:n.-87+16331G>T | |
| NM_024551.3:c.-87+28122G>T MANE Select | NP_078827.2:n.-87+28122G>T | |
| NM_001375363.1:c.-87+28122G>T | NP_001362292.1:n.-87+28122G>T | |
| NM_001375364.1:c.-248-16766G>T | NP_001362293.1:n.-248-16766G>T | |
| NM_001375365.1:c.-87+28100G>T | NP_001362294.1:n.-87+28100G>T |