HGVS | Genome Assembly |
---|---|
NC_000007.14:g.27095564C>A , CM000669.2:g.27095564C>A | GRCh38 |
NC_000007.13:g.27135183C>A , CM000669.1:g.27135183C>A | GRCh37 |
NC_000007.12:g.27101708C>A | NCBI36 |
NG_011813.1:g.5443G>T | |
NG_033087.1:g.4471C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000643460.2:c.349G>T MANE Select | ENSP00000494260.2:p.Ala117Ser | |
ENST00000343060.4:c.349G>T | ENSP00000343246.4:p.Ala117Ser | |
ENST00000355633.5:c.349G>T | ENSP00000347851.5:p.Ala117Ser | |
NM_005522.4:c.349G>T | NP_005513.1:p.Ala117Ser | |
NM_153620.2:c.349G>T | NP_705873.2:p.Ala117Ser | |
NM_005522.5:c.349G>T MANE Select | NP_005513.2:p.Ala117Ser | |
NM_153620.3:c.349G>T | NP_705873.3:p.Ala117Ser |