Linked Data
gnomAD v4:
2-113117807-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.113117807T>A , CM000664.2:g.113117807T>A | GRCh38 |
| NC_000002.11:g.113875384T>A , CM000664.1:g.113875384T>A | GRCh37 |
| NC_000002.10:g.113591855T>A | NCBI36 |
| NG_021240.1:g.4915T>A , LRG_188:g.4915T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409052.6:c.-272-2259T>A | ENSP00000387210.1:n.-272-2259T>A | |
| ENST00000465812.6:n.775+142T>A | ||
| ENST00000409052.5:c.-272-2259T>A | ENSP00000387210.1:n.-272-2259T>A | |
| XM_011511121.1:c.-272-2259T>A | XP_011509423.1:n.-272-2259T>A |