Linked Data
gnomAD v4:
13-48303754-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303754T>C , CM000675.2:g.48303754T>C | GRCh38 |
| NC_000013.10:g.48877890T>C , CM000675.1:g.48877890T>C | GRCh37 |
| NC_000013.9:g.47775891T>C | NCBI36 |
| NG_009009.1:g.5008T>C , LRG_517:g.5008T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.-159T>C MANE Select | ENSP00000267163.4:n.-159T>C | |
| ENST00000646097.1:c.-159T>C | ENSP00000496556.1:n.-159T>C | |
| ENST00000650461.1:c.-159T>C | ENSP00000497193.1:n.-159T>C | |
| ENST00000525036.1:n.4T>C | ||
| NM_000321.2:c.-159T>C , LRG_517t1:c.-159T>C | NP_000312.2:n.-159T>C | |
| NM_000321.3:c.-159T>C MANE Select | NP_000312.2:n.-159T>C |