Linked Data
gnomAD v4:
5-151259912-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151259912T>C , CM000667.2:g.151259912T>C | GRCh38 |
| NC_000005.9:g.150639473T>C , CM000667.1:g.150639473T>C | GRCh37 |
| NC_000005.8:g.150619666T>C | NCBI36 |
| NG_009059.1:g.11861T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357164.4:c.239T>C MANE Select | ENSP00000349687.3:p.Leu80Pro | |
| ENST00000357164.3:c.239T>C | ENSP00000349687.3:p.Leu80Pro | |
| ENST00000523004.1:c.114T>C | ||
| ENST00000523466.5:c.284T>C | ENSP00000429100.1:p.Leu95Pro | |
| NM_000405.4:c.239T>C | NP_000396.2:p.Leu80Pro | |
| NM_001167607.1:c.239T>C | NP_001161079.1:p.Leu80Pro | |
| NM_000405.5:c.239T>C MANE Select | NP_000396.2:p.Leu80Pro | |
| NM_001167607.2:c.239T>C | NP_001161079.1:p.Leu80Pro | |
| NM_001167607.3:c.239T>C | NP_001161079.1:p.Leu80Pro |