Linked Data
gnomAD v4:
2-113117884-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.113117884T>G , CM000664.2:g.113117884T>G | GRCh38 |
| NC_000002.11:g.113875461T>G , CM000664.1:g.113875461T>G | GRCh37 |
| NC_000002.10:g.113591932T>G | NCBI36 |
| NG_021240.1:g.4992T>G , LRG_188:g.4992T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409052.6:c.-272-2182T>G | ENSP00000387210.1:n.-272-2182T>G | |
| ENST00000465812.6:n.775+219T>G | ||
| ENST00000409052.5:c.-272-2182T>G | ENSP00000387210.1:n.-272-2182T>G | |
| XM_011511121.1:c.-272-2182T>G | XP_011509423.1:n.-272-2182T>G |