HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107663312G= , CM000669.2:g.107663312G= | GRCh38 |
NC_000007.13:g.107303757G= , CM000669.1:g.107303757G= | GRCh37 |
NC_000007.12:g.107090993G= | NCBI36 |
NG_008489.1:g.7678G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.181G= MANE Select | ENSP00000494017.1:p.Ala61= | |
ENST00000265715.7:c.181G= | ENSP00000265715.3:p.Ala61= | |
ENST00000440056.1:c.181G= | ENSP00000394760.1:p.Ala61= | |
NM_000441.1:c.181G= | NP_000432.1:p.Ala61= | |
XM_005250425.1:c.181G= | XP_005250482.1:p.Ala61= | |
XM_006716025.2:c.181G= | XP_006716088.1:p.Ala61= | |
XM_005250425.2:c.181G= | XP_005250482.1:p.Ala61= | |
XM_006716025.3:c.181G= | XP_006716088.1:p.Ala61= | |
XM_017012318.1:c.181G= | XP_016867807.1:p.Ala61= | |
NM_000441.2:c.181G= MANE Select | NP_000432.1:p.Ala61= |