Linked Data
gnomAD v4:
13-48380036-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48380036T>C , CM000675.2:g.48380036T>C | GRCh38 |
| NC_000013.10:g.48954172T>C , CM000675.1:g.48954172T>C | GRCh37 |
| NC_000013.9:g.47852173T>C | NCBI36 |
| NG_009009.1:g.81290T>C , LRG_517:g.81290T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.1390-17T>C MANE Select | ENSP00000267163.4:n.1390-17T>C | |
| ENST00000650461.1:c.1390-17T>C | ENSP00000497193.1:n.1390-17T>C | |
| ENST00000267163.4:c.1390-17T>C | ENSP00000267163.4:n.1390-17T>C | |
| NM_000321.2:c.1390-17T>C , LRG_517t1:c.1390-17T>C | NP_000312.2:n.1390-17T>C | |
| XM_011535171.1:c.1129-17T>C | XP_011533473.1:n.1129-17T>C | |
| XM_011535171.2:c.1129-17T>C | XP_011533473.1:n.1129-17T>C | |
| NM_000321.3:c.1390-17T>C MANE Select | NP_000312.2:n.1390-17T>C |