Linked Data
gnomAD v4:
13-48304017-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48304017G>T , CM000675.2:g.48304017G>T | GRCh38 |
| NC_000013.10:g.48878153G>T , CM000675.1:g.48878153G>T | GRCh37 |
| NC_000013.9:g.47776154G>T | NCBI36 |
| NG_009009.1:g.5271G>T , LRG_517:g.5271G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.105G>T MANE Select | ENSP00000267163.4:p.Gln35His | |
| ENST00000646097.1:c.105G>T | ENSP00000496556.1:p.Gln35His | |
| ENST00000650461.1:c.105G>T | ENSP00000497193.1:p.Gln35His | |
| ENST00000267163.4:c.105G>T | ENSP00000267163.4:p.Gln35His | |
| ENST00000467505.5:c.105G>T | ENSP00000434702.1:p.Gln35His | |
| ENST00000525036.1:n.267G>T | ||
| NM_000321.2:c.105G>T , LRG_517t1:c.105G>T | NP_000312.2:p.Gln35His | |
| NM_000321.3:c.105G>T MANE Select | NP_000312.2:p.Gln35His |