Linked Data
dbSNP Id:
rs201113897
gnomAD v4:
9-32550903-G-T
MyVariant Identifiers:
chr9:g.32550901G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.32550903G>T , CM000671.2:g.32550903G>T | GRCh38 |
| NC_000009.11:g.32550901G>T , CM000671.1:g.32550901G>T | GRCh37 |
| NC_000009.10:g.32540901G>T | NCBI36 |
| NG_017050.1:g.6722C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360538.7:c.69C>A MANE Select | ENSP00000353735.2:p.Pro23= | |
| ENST00000680198.1:c.69C>A | ENSP00000505143.1:p.Pro23= | |
| ENST00000681750.1:c.-174C>A | ENSP00000506413.1:n.-174C>A | |
| ENST00000360538.6:c.69C>A | ENSP00000353735.2:p.Pro23= | |
| ENST00000379858.1:c.3+1531C>A | ENSP00000369187.1:n.3+1531C>A | |
| NM_001195622.1:c.3+1531C>A | NP_001182551.1:n.3+1531C>A | |
| NM_005802.4:c.69C>A | NP_005793.2:p.Pro23= | |
| NM_005802.5:c.69C>A MANE Select | NP_005793.2:p.Pro23= | |
| NM_001195622.2:c.3+1531C>A | NP_001182551.1:n.3+1531C>A |