HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152307715G>A , CM000663.2:g.152307715G>A | GRCh38 |
NC_000001.10:g.152280191G>A , CM000663.1:g.152280191G>A | GRCh37 |
NC_000001.9:g.150546815G>A | NCBI36 |
NG_016190.1:g.22489C>T , LRG_1028:g.22489C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.7171C>T MANE Select | ENSP00000357789.1:p.Pro2391Ser | |
ENST00000368799.1:c.7171C>T | ENSP00000357789.1:p.Pro2391Ser | |
NM_002016.1:c.7171C>T , LRG_1028t1:c.7171C>T | NP_002007.1:p.Pro2391Ser | |
XM_011509329.1:c.7171C>T | XP_011507631.1:p.Pro2391Ser | |
NM_002016.2:c.7171C>T MANE Select | NP_002007.1:p.Pro2391Ser |