MyVariant.info:
GRCh37
chr11:g.17408499G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17386952G>T , CM000673.2:g.17386952G>T | GRCh38 |
| NC_000011.9:g.17408499G>T , CM000673.1:g.17408499G>T | GRCh37 |
| NC_000011.8:g.17365075G>T | NCBI36 |
| NG_012446.1:g.6708C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682350.1:c.879C>A | ENSP00000508090.1:p.Pro293= | |
| ENST00000682764.1:c.879C>A | ENSP00000506780.1:p.Pro293= | |
| ENST00000339994.5:c.1140C>A MANE Select | ENSP00000345708.4:p.Pro380= | |
| ENST00000339994.4:c.1140C>A | ENSP00000345708.4:p.Pro380= | |
| ENST00000528731.1:c.879C>A | ENSP00000434755.1:p.Pro293= | |
| NM_000525.3:c.1140C>A | NP_000516.3:p.Pro380= | |
| NM_001166290.1:c.879C>A | NP_001159762.1:p.Pro293= | |
| XM_006718226.2:c.879C>A | XP_006718289.1:p.Pro293= | |
| XR_930867.1:n.1298C>A | ||
| XM_006718226.3:c.879C>A | XP_006718289.1:p.Pro293= | |
| XM_017017680.1:c.879C>A | XP_016873169.1:p.Pro293= | |
| NM_001166290.2:c.879C>A | NP_001159762.1:p.Pro293= | |
| NM_001377296.1:c.879C>A | NP_001364225.1:p.Pro293= | |
| NM_001377297.1:c.879C>A | NP_001364226.1:p.Pro293= | |
| NM_000525.4:c.1140C>A MANE Select | NP_000516.3:p.Pro380= |