Linked Data
dbSNP Id:
rs1234583701
gnomAD v2:
2-48915889-A-C
gnomAD v3:
2-48688750-A-C
gnomAD v4:
2-48688750-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.48688750A>C , CM000664.2:g.48688750A>C | GRCh38 |
| NC_000002.11:g.48915889A>C , CM000664.1:g.48915889A>C | GRCh37 |
| NC_000002.10:g.48769393A>C | NCBI36 |
| NG_008193.1:g.71992T>G | |
| NG_033050.1:g.163826A>C | |
| NG_008193.2:g.71992T>G | |
| NG_033050.2:g.163826A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000294954.12:c.1047T>G (LHCGR) MANE Select | ENSP00000294954.6:p.Ala349= | |
| ENST00000294954.11:c.1047T>G (LHCGR) | ENSP00000294954.6:p.Ala349= | |
| ENST00000401907.5:c.948-611T>G (LHCGR) | ENSP00000385406.1:n.948-611T>G | |
| ENST00000402114.6:c.3441+17070A>C (STON1-GTF2A1L) | ENSP00000385701.1:n.3441+17070A>C | |
| ENST00000403273.5:c.948-167T>G (LHCGR) | ENSP00000385847.1:n.948-167T>G | |
| ENST00000405626.5:c.966T>G (LHCGR) | ENSP00000386033.1:p.Ala322= | |
| ENST00000508440.1:c.276+17070A>C (GTF2A1L) | ENSP00000421474.1:n.276+17070A>C | |
| ENST00000602369.3:c.*220+5474T>G | ENSP00000473498.1:n.*220+5474T>G | |
| NM_000233.3:c.1047T>G (LHCGR) | NP_000224.2:p.Ala349= | |
| NM_001198593.1:c.3441+17070A>C (STON1-GTF2A1L) | NP_001185522.1:n.3441+17070A>C | |
| XM_005264309.2:c.90T>G (LHCGR) | XP_005264366.1:p.Ala30= | |
| XM_006712015.2:c.117T>G (LHCGR) | XP_006712078.1:p.Ala39= | |
| XM_011532828.1:c.972T>G (LHCGR) | XP_011531130.1:p.Ala324= | |
| XM_011532829.1:c.786T>G (LHCGR) | XP_011531131.1:p.Ala262= | |
| XM_011532830.1:c.705T>G (LHCGR) | XP_011531132.1:p.Ala235= | |
| XM_011532831.1:c.411T>G (LHCGR) | XP_011531133.1:p.Ala137= | |
| XM_011532832.1:c.117T>G (LHCGR) | XP_011531134.1:p.Ala39= | |
| XM_011532833.1:c.117T>G (LHCGR) | XP_011531135.1:p.Ala39= | |
| XM_011532834.1:c.90T>G (LHCGR) | XP_011531136.1:p.Ala30= | |
| XM_005264309.3:c.90T>G (LHCGR) | XP_005264366.1:p.Ala30= | |
| XM_006712015.3:c.117T>G (LHCGR) | XP_006712078.1:p.Ala39= | |
| XM_011532834.2:c.90T>G (LHCGR) | XP_011531136.1:p.Ala30= | |
| XM_017004089.1:c.792T>G (LHCGR) | XP_016859578.1:p.Ala264= | |
| XM_017004090.1:c.411T>G (LHCGR) | XP_016859579.1:p.Ala137= | |
| NM_000233.4:c.1047T>G (LHCGR) MANE Select | NP_000224.2:p.Ala349= | |
| NM_001198593.2:c.3441+17070A>C (STON1-GTF2A1L) | NP_001185522.1:n.3441+17070A>C |