HGVS | Genome Assembly |
---|---|
NC_000005.10:g.96429231T>G , CM000667.2:g.96429231T>G | GRCh38 |
NC_000005.9:g.95764935T>G , CM000667.1:g.95764935T>G | GRCh37 |
NC_000005.8:g.95790691T>G | NCBI36 |
NG_021161.1:g.9051A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311106.8:c.267A>C MANE Select | ENSP00000308024.2:p.Arg89Ser | |
ENST00000311106.7:c.267A>C | ENSP00000308024.2:p.Arg89Ser | |
ENST00000508626.5:c.126A>C | ENSP00000421600.1:p.Arg42Ser | |
ENST00000509190.1:c.267A>C | ENSP00000427294.1:p.Arg89Ser | |
NM_000439.4:c.267A>C | NP_000430.3:p.Arg89Ser | |
NM_001177875.1:c.126A>C | NP_001171346.1:p.Arg42Ser | |
NR_130776.1:n.354+49579T>G | ||
NM_000439.5:c.267A>C MANE Select | NP_000430.3:p.Arg89Ser | |
NM_001177875.2:c.126A>C | NP_001171346.1:p.Arg42Ser |