Linked Data
dbSNP Id:
rs755222188
ExAC:
6:129802541 G / T
gnomAD v2:
6-129802541-G-T
gnomAD v4:
6-129481396-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.129481396G>T , CM000668.2:g.129481396G>T | GRCh38 |
| NC_000006.11:g.129802541G>T , CM000668.1:g.129802541G>T | GRCh37 |
| NC_000006.10:g.129844234G>T | NCBI36 |
| NG_008678.1:g.603256G>T , LRG_409:g.603256G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617695.5:c.7694G>T | ENSP00000481744.2:p.Gly2565Val | |
| ENST00000618192.5:c.7970G>T | ENSP00000480802.2:p.Gly2657Val | |
| ENST00000421865.3:c.7706G>T MANE Select | ENSP00000400365.2:p.Gly2569Val | |
| ENST00000421865.2:c.7706G>T | ENSP00000400365.2:p.Gly2569Val | |
| ENST00000617695.4:c.7694G>T | ENSP00000481744.1:p.Gly2565Val | |
| ENST00000618192.4:c.7703G>T | ENSP00000480802.1:p.Gly2568Val | |
| NM_000426.3:c.7706G>T , LRG_409t1:c.7706G>T | NP_000417.2:p.Gly2569Val | |
| NM_001079823.1:c.7694G>T | NP_001073291.1:p.Gly2565Val | |
| XM_005266981.2:c.7970G>T | XP_005267038.1:p.Gly2657Val | |
| XM_005266982.2:c.7958G>T | XP_005267039.1:p.Gly2653Val | |
| XM_011535820.1:c.7964G>T | XP_011534122.1:p.Gly2655Val | |
| XM_005266981.3:c.7970G>T | XP_005267038.1:p.Gly2657Val | |
| XM_005266982.3:c.7958G>T | XP_005267039.1:p.Gly2653Val | |
| XM_011535820.2:c.7964G>T | XP_011534122.1:p.Gly2655Val | |
| XM_017010851.2:c.7976G>T | XP_016866340.1:p.Gly2659Val | |
| XM_017010852.1:c.6101G>T | XP_016866341.1:p.Gly2034Val | |
| NM_000426.4:c.7706G>T MANE Select | NP_000417.3:p.Gly2569Val | |
| NM_001079823.2:c.7694G>T | NP_001073291.2:p.Gly2565Val |