Linked Data
gnomAD v4:
9-32550934-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.32550934C>A , CM000671.2:g.32550934C>A | GRCh38 |
| NC_000009.11:g.32550932C>A , CM000671.1:g.32550932C>A | GRCh37 |
| NC_000009.10:g.32540932C>A | NCBI36 |
| NG_017050.1:g.6691G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360538.7:c.38G>T MANE Select | ENSP00000353735.2:p.Arg13Leu | |
| ENST00000680198.1:c.38G>T | ENSP00000505143.1:p.Arg13Leu | |
| ENST00000681750.1:c.-205G>T | ENSP00000506413.1:n.-205G>T | |
| ENST00000360538.6:c.38G>T | ENSP00000353735.2:p.Arg13Leu | |
| ENST00000379858.1:c.3+1500G>T | ENSP00000369187.1:n.3+1500G>T | |
| NM_001195622.1:c.3+1500G>T | NP_001182551.1:n.3+1500G>T | |
| NM_005802.4:c.38G>T | NP_005793.2:p.Arg13Leu | |
| NM_005802.5:c.38G>T MANE Select | NP_005793.2:p.Arg13Leu | |
| NM_001195622.2:c.3+1500G>T | NP_001182551.1:n.3+1500G>T |