MyVariant.info:
GRCh37
chr2:g.179721046G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178856319G>T , CM000664.2:g.178856319G>T | GRCh38 |
| NC_000002.11:g.179721046G>T , CM000664.1:g.179721046G>T | GRCh37 |
| NC_000002.10:g.179429291G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000443758.7:c.2803C>A MANE Select | ENSP00000390190.2:p.Arg935= | |
| ENST00000443758.6:c.2803C>A | ENSP00000390190.2:p.Arg935= | |
| ENST00000343876.6:c.1135C>A | ENSP00000344627.2:p.Arg379= | |
| ENST00000420890.6:c.2803C>A | ENSP00000395995.2:p.Arg935= | |
| ENST00000443758.5:c.2803C>A | ENSP00000390190.1:p.Arg935= | |
| NM_173648.3:c.2803C>A | NP_775919.3:p.Arg935= | |
| XM_011510991.1:c.2803C>A | XP_011509293.1:p.Arg935= | |
| XM_011510992.1:c.2803C>A | XP_011509294.1:p.Arg935= | |
| XM_011510993.1:c.2623C>A | XP_011509295.1:p.Arg875= | |
| XM_011510994.1:c.859C>A | XP_011509296.1:p.Arg287= | |
| XR_923628.1:n.1352+27665G>T | ||
| XM_011510991.3:c.2803C>A | XP_011509293.1:p.Arg935= | |
| XM_011510992.3:c.2803C>A | XP_011509294.1:p.Arg935= | |
| XM_011510993.3:c.2623C>A | XP_011509295.1:p.Arg875= | |
| XM_017003867.2:c.2803C>A | XP_016859356.1:p.Arg935= | |
| XM_017003868.2:c.2803C>A | XP_016859357.1:p.Arg935= | |
| XM_017003869.2:c.2803C>A | XP_016859358.1:p.Arg935= | |
| XM_017003870.2:c.1513C>A | XP_016859359.1:p.Arg505= | |
| XM_017003871.1:c.859C>A | XP_016859360.1:p.Arg287= | |
| XR_001738715.2:n.2992C>A | ||
| NM_173648.4:c.2803C>A MANE Select | NP_775919.3:p.Arg935= |