Linked Data
dbSNP Id:
rs771288619
ExAC:
10:69970222 G / T
gnomAD v2:
10-69970222-G-T
gnomAD v4:
10-68210465-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68210465G>T , CM000672.2:g.68210465G>T | GRCh38 |
| NC_000010.10:g.69970222G>T , CM000672.1:g.69970222G>T | GRCh37 |
| NC_000010.9:g.69640228G>T | NCBI36 |
| NG_032118.1:g.109349G>T , LRG_410:g.109349G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354393.7:c.*10G>T | ENSP00000346369.2:n.*10G>T | |
| ENST00000540630.6:c.*10G>T | ENSP00000441668.3:n.*10G>T | |
| ENST00000613327.5:c.*10G>T | ENSP00000480757.2:n.*10G>T | |
| ENST00000688812.1:c.*1236G>T | ENSP00000510658.1:n.*1236G>T | |
| ENST00000690544.1:c.*3244G>T | ENSP00000508989.1:n.*3244G>T | |
| ENST00000358913.10:c.*10G>T MANE Select | ENSP00000351790.5:n.*10G>T | |
| ENST00000354393.6:c.*10G>T | ENSP00000346369.2:n.*10G>T | |
| ENST00000358913.9:c.*10G>T | ENSP00000351790.5:n.*10G>T | |
| ENST00000540630.5:c.*10G>T | ENSP00000441668.2:n.*10G>T | |
| ENST00000613327.4:c.*10G>T | ENSP00000480757.1:n.*10G>T | |
| NM_001256267.1:c.*10G>T | NP_001243196.1:n.*10G>T | |
| NM_001256268.1:c.*10G>T | NP_001243197.1:n.*10G>T | |
| NM_032578.3:c.*10G>T , LRG_410t1:c.*10G>T | NP_115967.2:n.*10G>T | |
| NR_045662.3:n.3400G>T | ||
| NR_045663.3:n.4102G>T | ||
| XM_006718043.2:c.*10G>T | XP_006718106.1:n.*10G>T | |
| XM_011540292.1:c.*10G>T | XP_011538594.1:n.*10G>T | |
| XR_946029.1:n.1574+4823C>A | ||
| XM_017016833.1:c.*10G>T | XP_016872322.1:n.*10G>T | |
| XM_017016834.2:c.*10G>T | XP_016872323.1:n.*10G>T | |
| XM_024448236.1:c.*10G>T | XP_024304004.1:n.*10G>T | |
| NR_045662.4:n.3510G>T | ||
| NR_045663.4:n.4047G>T | ||
| NM_001256267.2:c.*10G>T | NP_001243196.1:n.*10G>T | |
| NM_001256268.2:c.*10G>T | NP_001243197.1:n.*10G>T | |
| NM_032578.4:c.*10G>T MANE Select | NP_115967.2:n.*10G>T |