HGVS | Genome Assembly |
---|---|
NC_000020.11:g.6770374A>C , CM000682.2:g.6770374A>C | GRCh38 |
NC_000020.10:g.6751021A>C , CM000682.1:g.6751021A>C | GRCh37 |
NC_000020.9:g.6699021A>C | NCBI36 |
NG_023233.1:g.7277A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378827.5:c.248A>C MANE Select | ENSP00000368104.3:p.Tyr83Ser | |
ENST00000378827.4:c.248A>C | ENSP00000368104.3:p.Tyr83Ser | |
NM_001200.2:c.248A>C | NP_001191.1:p.Tyr83Ser | |
XM_011529323.1:c.-123+1499A>C | XP_011527625.1:n.-123+1499A>C | |
NM_001200.3:c.248A>C | NP_001191.1:p.Tyr83Ser | |
NM_001200.4:c.248A>C MANE Select | NP_001191.1:p.Tyr83Ser |