MyVariant.info:
GRCh37
chr6:g.129824341A>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.129503196A>C , CM000668.2:g.129503196A>C | GRCh38 |
| NC_000006.11:g.129824341A>C , CM000668.1:g.129824341A>C | GRCh37 |
| NC_000006.10:g.129866034A>C | NCBI36 |
| NG_008678.1:g.625056A>C , LRG_409:g.625056A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494137.2:c.528A>C | ENSP00000510626.1:p.Gly176= | |
| ENST00000498257.6:c.528A>C | ENSP00000510533.1:p.Gly176= | |
| ENST00000617695.5:c.8451A>C | ENSP00000481744.2:p.Gly2817= | |
| ENST00000618192.5:c.8727A>C | ENSP00000480802.2:p.Gly2909= | |
| ENST00000688198.1:n.1441A>C | ||
| ENST00000688799.1:c.528A>C | ENSP00000508458.1:p.Gly176= | |
| ENST00000690858.1:n.1457A>C | ||
| ENST00000693461.1:n.800A>C | ||
| ENST00000421865.3:c.8463A>C MANE Select | ENSP00000400365.2:p.Gly2821= | |
| ENST00000421865.2:c.8463A>C | ENSP00000400365.2:p.Gly2821= | |
| ENST00000617695.4:c.8451A>C | ENSP00000481744.1:p.Gly2817= | |
| ENST00000618192.4:c.8460A>C | ENSP00000480802.1:p.Gly2820= | |
| NM_000426.3:c.8463A>C , LRG_409t1:c.8463A>C | NP_000417.2:p.Gly2821= | |
| NM_001079823.1:c.8451A>C | NP_001073291.1:p.Gly2817= | |
| XM_005266981.2:c.8727A>C | XP_005267038.1:p.Gly2909= | |
| XM_005266982.2:c.8715A>C | XP_005267039.1:p.Gly2905= | |
| XM_011535820.1:c.8721A>C | XP_011534122.1:p.Gly2907= | |
| XR_942984.1:n.1461-405T>G | ||
| XR_942985.1:n.1325-405T>G | ||
| XM_005266981.3:c.8727A>C | XP_005267038.1:p.Gly2909= | |
| XM_005266982.3:c.8715A>C | XP_005267039.1:p.Gly2905= | |
| XM_011535820.2:c.8721A>C | XP_011534122.1:p.Gly2907= | |
| XM_017010851.2:c.8733A>C | XP_016866340.1:p.Gly2911= | |
| XM_017010852.1:c.6858A>C | XP_016866341.1:p.Gly2286= | |
| XR_001743859.1:n.3901-405T>G | ||
| XR_001743860.1:n.1180-405T>G | ||
| XR_001743861.1:n.1347-405T>G | ||
| XR_001743863.1:n.883-405T>G | ||
| XR_002956395.1:n.9132-405T>G | ||
| XR_002956396.1:n.3127-405T>G | ||
| NM_000426.4:c.8463A>C MANE Select | NP_000417.3:p.Gly2821= | |
| NM_001079823.2:c.8451A>C | NP_001073291.2:p.Gly2817= |