Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155070881G>C , CM000669.2:g.155070881G>C | GRCh38 |
| NC_000007.13:g.154862591G>C , CM000669.1:g.154862591G>C | GRCh37 |
| NC_000007.12:g.154493524G>C | NCBI36 |
| NG_044997.1:g.5558G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287907.3:c.-19G>C (HTR5A) MANE Select | ENSP00000287907.2:n.-19G>C | |
| ENST00000287907.2:c.-19G>C (HTR5A) | ENSP00000287907.2:n.-19G>C | |
| NM_024012.3:c.-19G>C (HTR5A) | NP_076917.1:n.-19G>C | |
| NR_038945.1:n.524+153C>G (HTR5A-AS1) | ||
| NM_024012.4:c.-19G>C (HTR5A) MANE Select | NP_076917.1:n.-19G>C |