Linked Data
gnomAD v4:
9-137199534-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137199534G>T , CM000671.2:g.137199534G>T | GRCh38 |
| NC_000009.11:g.140093986G>T , CM000671.1:g.140093986G>T | GRCh37 |
| NC_000009.10:g.139213807G>T | NCBI36 |
| NG_027801.1:g.6178C>A | |
| NG_027801.2:g.9660C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409012.6:c.1178C>A MANE Select | ENSP00000387100.4:p.Ala393Glu | |
| ENST00000333046.8:c.572C>A | ENSP00000327617.4:p.Ala191Glu | |
| ENST00000409012.4:c.1178C>A | ENSP00000387100.4:p.Ala393Glu | |
| ENST00000541945.1:n.90+4570C>A | ||
| NM_001128228.2:c.1178C>A | NP_001121700.2:p.Ala393Glu | |
| NM_001128228.3:c.1178C>A MANE Select | NP_001121700.2:p.Ala393Glu |