HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20759889C>T , CM000686.2:g.20759889C>T | GRCh38 |
NC_000024.9:g.22921775C>T , CM000686.1:g.22921775C>T | GRCh37 |
NC_000024.8:g.21331163C>T | NCBI36 |
NG_032924.1:g.8822C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000629237.2:c.103C>T MANE Select | ENSP00000486252.1:p.Pro35Ser | |
ENST00000629237.1:c.103C>T | ENSP00000486252.1:p.Pro35Ser | |
NM_001039567.2:c.103C>T | NP_001034656.1:p.Pro35Ser | |
XM_011531423.1:c.52C>T | XP_011529725.1:p.Pro18Ser | |
NM_001039567.3:c.103C>T MANE Select | NP_001034656.1:p.Pro35Ser |