MyVariant.info:
GRCh37
chr1:g.47398441T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.46932769T>C , CM000663.2:g.46932769T>C | GRCh38 |
| NC_000001.10:g.47398441T>C , CM000663.1:g.47398441T>C | GRCh37 |
| NC_000001.9:g.47171028T>C | NCBI36 |
| NG_007932.1:g.13716A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310638.9:c.1356A>G MANE Select | ENSP00000311095.4:p.Gly452= | |
| ENST00000310638.8:c.1356A>G | ENSP00000311095.4:p.Gly452= | |
| ENST00000371904.8:c.1359A>G | ENSP00000360971.4:p.Gly453= | |
| ENST00000371905.1:c.1356A>G | ENSP00000360972.1:p.Gly452= | |
| ENST00000462347.5:c.1062A>G | ENSP00000477495.1:p.Gly354= | |
| ENST00000465874.5:c.*154A>G | ENSP00000476368.1:n.*154A>G | |
| ENST00000468629.5:c.*61A>G | ENSP00000476619.1:n.*61A>G | |
| ENST00000474458.5:c.*61A>G | ENSP00000476988.1:n.*61A>G | |
| ENST00000475477.5:c.*150A>G | ENSP00000476854.1:n.*150A>G | |
| NM_000778.3:c.1356A>G | NP_000769.2:p.Gly452= | |
| XM_005270539.1:c.1062A>G | XP_005270596.1:p.Gly354= | |
| XM_011540826.1:c.1374A>G | XP_011539128.1:p.Gly458= | |
| XM_011540827.1:c.1080A>G | XP_011539129.1:p.Gly360= | |
| XM_011540828.1:c.1062A>G | XP_011539130.1:p.Gly354= | |
| XR_246241.1:n.1260A>G | ||
| XR_246242.1:n.1244A>G | ||
| NM_001319155.1:c.1260A>G | NP_001306084.1:p.Gly420= | |
| NM_001363587.1:c.1062A>G | NP_001350516.1:p.Gly354= | |
| NR_134988.1:n.1061A>G | ||
| NR_134989.1:n.1252A>G | ||
| NR_134990.1:n.1246A>G | ||
| NR_134991.1:n.1233A>G | ||
| NR_134992.1:n.862A>G | ||
| NR_134993.1:n.996A>G | ||
| NR_134994.1:n.1268A>G | ||
| XM_017000465.1:c.1044A>G | XP_016855954.1:p.Gly348= | |
| XR_001737005.1:n.1334A>G | ||
| NM_000778.4:c.1356A>G MANE Select | NP_000769.2:p.Gly452= | |
| NM_001319155.2:c.1260A>G | NP_001306084.1:p.Gly420= | |
| NM_001363587.2:c.1062A>G | NP_001350516.1:p.Gly354= | |
| NR_134988.2:n.1053A>G | ||
| NR_134989.2:n.1244A>G | ||
| NR_134990.2:n.1238A>G | ||
| NR_134991.2:n.1225A>G | ||
| NR_134992.2:n.854A>G | ||
| NR_134993.2:n.988A>G | ||
| NR_134994.2:n.1260A>G |