Linked Data
MyVariant Identifiers:
chr5:g.150639465T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151259904T>C , CM000667.2:g.151259904T>C | GRCh38 |
| NC_000005.9:g.150639465T>C , CM000667.1:g.150639465T>C | GRCh37 |
| NC_000005.8:g.150619658T>C | NCBI36 |
| NG_009059.1:g.11853T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357164.4:c.231T>C MANE Select | ENSP00000349687.3:p.Ser77= | |
| ENST00000357164.3:c.231T>C | ENSP00000349687.3:p.Ser77= | |
| ENST00000523004.1:c.106T>C | ||
| ENST00000523466.5:c.276T>C | ENSP00000429100.1:p.Ser92= | |
| NM_000405.4:c.231T>C | NP_000396.2:p.Ser77= | |
| NM_001167607.1:c.231T>C | NP_001161079.1:p.Ser77= | |
| NM_000405.5:c.231T>C MANE Select | NP_000396.2:p.Ser77= | |
| NM_001167607.2:c.231T>C | NP_001161079.1:p.Ser77= | |
| NM_001167607.3:c.231T>C | NP_001161079.1:p.Ser77= |