HGVS | Genome Assembly |
---|---|
NC_000022.11:g.45295657T>C , CM000684.2:g.45295657T>C | GRCh38 |
NC_000022.10:g.45691538T>C , CM000684.1:g.45691538T>C | GRCh37 |
NC_000022.9:g.44070202T>C | NCBI36 |
NG_016203.1:g.15671T>C | |
NG_016203.2:g.15671T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216211.9:c.802T>C MANE Select | ENSP00000216211.4:p.Ser268Pro | |
ENST00000216211.8:c.802T>C | ENSP00000216211.4:p.Ser268Pro | |
ENST00000396082.2:c.439T>C | ENSP00000379391.2:p.Ser147Pro | |
NM_001167574.1:c.439T>C | NP_001161046.1:p.Ser147Pro | |
NM_006953.3:c.802T>C | NP_008884.1:p.Ser268Pro | |
XM_011530364.1:c.808T>C | XP_011528666.1:p.Ser270Pro | |
XM_011530365.1:c.445T>C | XP_011528667.1:p.Ser149Pro | |
NM_006953.4:c.802T>C MANE Select | NP_008884.1:p.Ser268Pro | |
NM_001167574.2:c.439T>C | NP_001161046.1:p.Ser147Pro |