Linked Data
gnomAD v4:
2-113117895-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.113117895G>T , CM000664.2:g.113117895G>T | GRCh38 |
| NC_000002.11:g.113875472G>T , CM000664.1:g.113875472G>T | GRCh37 |
| NC_000002.10:g.113591943G>T | NCBI36 |
| NG_021240.1:g.5003G>T , LRG_188:g.5003G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409052.6:c.-272-2171G>T | ENSP00000387210.1:n.-272-2171G>T | |
| ENST00000465812.6:n.775+230G>T | ||
| ENST00000361779.7:c.-343G>T | ENSP00000354816.3:n.-343G>T | |
| ENST00000409052.5:c.-272-2171G>T | ENSP00000387210.1:n.-272-2171G>T | |
| NM_000577.4:c.-124G>T | NP_000568.1:n.-124G>T | |
| NM_173841.2:c.-124G>T , LRG_188t1:c.-124G>T | NP_776213.1:n.-124G>T | |
| NM_173843.2:c.-343G>T | NP_776215.1:n.-343G>T | |
| XM_011511121.1:c.-272-2171G>T | XP_011509423.1:n.-272-2171G>T | |
| NM_001318914.1:c.-406G>T | NP_001305843.1:n.-406G>T |