HGVS | Genome Assembly |
---|---|
NC_000001.11:g.203183684T>G , CM000663.2:g.203183684T>G | GRCh38 |
NC_000001.10:g.203152812T>G , CM000663.1:g.203152812T>G | GRCh37 |
NC_000001.9:g.201419435T>G | NCBI36 |
NG_013056.1:g.8111A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000255409.8:c.422A>C MANE Select | ENSP00000255409.3:p.Tyr141Ser | |
ENST00000255409.7:c.422A>C | ENSP00000255409.3:p.Tyr141Ser | |
NM_001276.2:c.422A>C | NP_001267.2:p.Tyr141Ser | |
XM_011509105.1:c.440A>C | XP_011507407.1:p.Tyr147Ser | |
XM_011509106.1:c.440A>C | XP_011507408.1:p.Tyr147Ser | |
XM_011509107.1:c.422A>C | XP_011507409.1:p.Tyr141Ser | |
XM_011509108.1:c.440A>C | XP_011507410.1:p.Tyr147Ser | |
NM_001276.3:c.422A>C | NP_001267.2:p.Tyr141Ser | |
NM_001276.4:c.422A>C MANE Select | NP_001267.2:p.Tyr141Ser |