Linked Data
gnomAD v4:
13-48303759-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303759G>T , CM000675.2:g.48303759G>T | GRCh38 |
| NC_000013.10:g.48877895G>T , CM000675.1:g.48877895G>T | GRCh37 |
| NC_000013.9:g.47775896G>T | NCBI36 |
| NG_009009.1:g.5013G>T , LRG_517:g.5013G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.-154G>T MANE Select | ENSP00000267163.4:n.-154G>T | |
| ENST00000646097.1:c.-154G>T | ENSP00000496556.1:n.-154G>T | |
| ENST00000650461.1:c.-154G>T | ENSP00000497193.1:n.-154G>T | |
| ENST00000525036.1:n.9G>T | ||
| NM_000321.2:c.-154G>T , LRG_517t1:c.-154G>T | NP_000312.2:n.-154G>T | |
| NM_000321.3:c.-154G>T MANE Select | NP_000312.2:n.-154G>T |