Linked Data
gnomAD v4:
4-46993575-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.46993575G>T , CM000666.2:g.46993575G>T | GRCh38 |
| NC_000004.11:g.46995592G>T , CM000666.1:g.46995592G>T | GRCh37 |
| NC_000004.10:g.46690349G>T | NCBI36 |
| NG_011809.1:g.4989C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264318.4:c.-151C>A (GABRA4) MANE Select | ENSP00000264318.3:n.-151C>A | |
| ENST00000264318.3:c.-151C>A (GABRA4) | ENSP00000264318.3:n.-151C>A | |
| NM_000809.3:c.-151C>A (GABRA4) | NP_000800.2:n.-151C>A | |
| XM_011513677.1:c.-151C>A (GABRA4) | XP_011511979.1:n.-151C>A | |
| XM_024453977.1:c.-443G>T (GABRB1) | XP_024309745.1:n.-443G>T | |
| NM_000809.4:c.-151C>A (GABRA4) MANE Select | NP_000800.2:n.-151C>A | |
| NM_001204266.2:c.-140C>A (GABRA4) | NP_001191195.1:n.-140C>A | |
| NM_001204267.2:c.-140C>A (GABRA4) | NP_001191196.1:n.-140C>A |