Linked Data
dbSNP Id:
rs1354805701
gnomAD v2:
15-73614902-G-T
gnomAD v4:
15-73322561-G-T
MyVariant Identifiers:
chr15:g.73614902G>T (hg19)
chr15:g.73614902_73614903delinsTC (hg19)
chr15:g.73322561G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322561G>T , CM000677.2:g.73322561G>T | GRCh38 |
| NC_000015.9:g.73614902G>T , CM000677.1:g.73614902G>T | GRCh37 |
| NC_000015.8:g.71401955G>T | NCBI36 |
| NG_009063.1:g.51704C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3532C>A MANE Select | ENSP00000261917.3:p.Pro1178Thr | |
| ENST00000261917.3:c.3532C>A | ENSP00000261917.3:p.Pro1178Thr | |
| NM_005477.2:c.3532C>A | NP_005468.1:p.Pro1178Thr | |
| XM_011521148.1:c.2314C>A | XP_011519450.1:p.Pro772Thr | |
| XM_011521148.2:c.2314C>A | XP_011519450.1:p.Pro772Thr | |
| NM_005477.3:c.3532C>A MANE Select | NP_005468.1:p.Pro1178Thr |