Linked Data
dbSNP Id:
rs977700501
gnomAD v2:
2-48921314-A-G
gnomAD v3:
2-48694175-A-G
gnomAD v4:
2-48694175-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.48694175A>G , CM000664.2:g.48694175A>G | GRCh38 |
| NC_000002.11:g.48921314A>G , CM000664.1:g.48921314A>G | GRCh37 |
| NC_000002.10:g.48774818A>G | NCBI36 |
| NG_008193.1:g.66567T>C | |
| NG_033050.1:g.169251A>G | |
| NG_008193.2:g.66567T>C | |
| NG_033050.2:g.169251A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000294954.12:c.947+49T>C (LHCGR) MANE Select | ENSP00000294954.6:n.947+49T>C | |
| ENST00000294954.11:c.947+49T>C (LHCGR) | ENSP00000294954.6:n.947+49T>C | |
| ENST00000401907.5:c.947+49T>C (LHCGR) | ENSP00000385406.1:n.947+49T>C | |
| ENST00000402114.6:c.3441+22495A>G (STON1-GTF2A1L) | ENSP00000385701.1:n.3441+22495A>G | |
| ENST00000403273.5:c.947+49T>C (LHCGR) | ENSP00000385847.1:n.947+49T>C | |
| ENST00000405626.5:c.866+4440T>C (LHCGR) | ENSP00000386033.1:n.866+4440T>C | |
| ENST00000508440.1:c.276+22495A>G (GTF2A1L) | ENSP00000421474.1:n.276+22495A>G | |
| ENST00000602369.3:c.*220+49T>C | ENSP00000473498.1:n.*220+49T>C | |
| NM_000233.3:c.947+49T>C (LHCGR) | NP_000224.2:n.947+49T>C | |
| NM_001198593.1:c.3441+22495A>G (STON1-GTF2A1L) | NP_001185522.1:n.3441+22495A>G | |
| XM_005264309.2:c.-11+66T>C (LHCGR) | XP_005264366.1:n.-11+66T>C | |
| XM_006712015.2:c.-911T>C (LHCGR) | XP_006712078.1:n.-911T>C | |
| XM_011532828.1:c.872+49T>C (LHCGR) | XP_011531130.1:n.872+49T>C | |
| XM_011532829.1:c.686+49T>C (LHCGR) | XP_011531131.1:n.686+49T>C | |
| XM_011532830.1:c.606-5326T>C (LHCGR) | XP_011531132.1:n.606-5326T>C | |
| XM_011532831.1:c.311+49T>C (LHCGR) | XP_011531133.1:n.311+49T>C | |
| XM_011532832.1:c.-478T>C (LHCGR) | XP_011531134.1:n.-478T>C | |
| XM_011532833.1:c.-474T>C (LHCGR) | XP_011531135.1:n.-474T>C | |
| XM_011532834.1:c.-280T>C (LHCGR) | XP_011531136.1:n.-280T>C | |
| XM_005264309.3:c.-11+66T>C (LHCGR) | XP_005264366.1:n.-11+66T>C | |
| XM_006712015.3:c.-911T>C (LHCGR) | XP_006712078.1:n.-911T>C | |
| XM_011532834.2:c.-280T>C (LHCGR) | XP_011531136.1:n.-280T>C | |
| XM_017004089.1:c.692+49T>C (LHCGR) | XP_016859578.1:n.692+49T>C | |
| XM_017004090.1:c.311+49T>C (LHCGR) | XP_016859579.1:n.311+49T>C | |
| NM_000233.4:c.947+49T>C (LHCGR) MANE Select | NP_000224.2:n.947+49T>C | |
| NM_001198593.2:c.3441+22495A>G (STON1-GTF2A1L) | NP_001185522.1:n.3441+22495A>G |