Linked Data
dbSNP Id:
rs1577805167
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.46993573T>G , CM000666.2:g.46993573T>G | GRCh38 |
| NC_000004.11:g.46995590T>G , CM000666.1:g.46995590T>G | GRCh37 |
| NC_000004.10:g.46690347T>G | NCBI36 |
| NG_011809.1:g.4991A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264318.4:c.-149A>C (GABRA4) MANE Select | ENSP00000264318.3:n.-149A>C | |
| ENST00000264318.3:c.-149A>C (GABRA4) | ENSP00000264318.3:n.-149A>C | |
| NM_000809.3:c.-149A>C (GABRA4) | NP_000800.2:n.-149A>C | |
| XM_011513677.1:c.-149A>C (GABRA4) | XP_011511979.1:n.-149A>C | |
| XM_024453977.1:c.-445T>G (GABRB1) | XP_024309745.1:n.-445T>G | |
| NM_000809.4:c.-149A>C (GABRA4) MANE Select | NP_000800.2:n.-149A>C | |
| NM_001204266.2:c.-138A>C (GABRA4) | NP_001191195.1:n.-138A>C | |
| NM_001204267.2:c.-138A>C (GABRA4) | NP_001191196.1:n.-138A>C |