MyVariant.info:
GRCh37
chr18:g.10715677G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.10715679G>T , CM000680.2:g.10715679G>T | GRCh38 |
| NC_000018.9:g.10715677G>T , CM000680.1:g.10715677G>T | GRCh37 |
| NC_000018.8:g.10705677G>T | NCBI36 |
| NG_034005.1:g.438084C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000383408.7:c.5128C>A | ENSP00000372900.4:p.Arg1710= | |
| ENST00000686869.1:n.5185C>A | ||
| ENST00000674853.1:c.5227C>A MANE Select | ENSP00000501957.1:p.Arg1743= | |
| ENST00000302079.10:c.5053C>A | ENSP00000303316.6:p.Arg1685= | |
| ENST00000383408.6:c.4906C>A | ENSP00000372900.3:p.Arg1636= | |
| ENST00000503781.7:c.5053C>A | ENSP00000421377.3:p.Arg1685= | |
| ENST00000580640.5:c.5128C>A | ENSP00000463094.1:p.Arg1710= | |
| ENST00000582913.5:c.5094C>A | ENSP00000462115.1:n.5094C>A | |
| NM_022068.3:c.5053C>A | NP_071351.2:p.Arg1685= | |
| XM_011525723.1:c.5185C>A | XP_011524025.1:p.Arg1729= | |
| XM_011525724.1:c.5128C>A | XP_011524026.1:p.Arg1710= | |
| XM_011525725.1:c.5095C>A | XP_011524027.1:p.Arg1699= | |
| XM_011525726.1:c.5185C>A | XP_011524028.1:p.Arg1729= | |
| XM_011525723.3:c.5185C>A | XP_011524025.1:p.Arg1729= | |
| XM_011525724.3:c.5128C>A | XP_011524026.1:p.Arg1710= | |
| XM_011525725.3:c.5095C>A | XP_011524027.1:p.Arg1699= | |
| XM_011525726.3:c.5185C>A | XP_011524028.1:p.Arg1729= | |
| XM_017025918.2:c.5146C>A | XP_016881407.1:p.Arg1716= | |
| XR_001753259.2:n.6182C>A | ||
| NM_001378183.1:c.5227C>A MANE Select | NP_001365112.1:p.Arg1743= | |
| NM_022068.4:c.5053C>A | NP_071351.2:p.Arg1685= |