HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202556345C>T , CM000664.2:g.202556345C>T | GRCh38 |
NC_000002.11:g.203421068C>T , CM000664.1:g.203421068C>T | GRCh37 |
NC_000002.10:g.203129313C>T | NCBI36 |
NG_009363.1:g.185019C>T , LRG_712:g.185019C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.2680C>T MANE Select | ENSP00000363708.4:p.Pro894Ser | |
ENST00000638587.1:c.2611C>T | ENSP00000491062.1:n.2611C>T | |
ENST00000374574.2:c.1587-3351C>T | ENSP00000363702.2:n.1587-3351C>T | |
ENST00000374580.8:c.2680C>T | ENSP00000363708.4:p.Pro894Ser | |
NM_001204.6:c.2680C>T , LRG_712t1:c.2680C>T | NP_001195.2:p.Pro894Ser | |
XM_011511687.1:c.2680C>T | XP_011509989.1:p.Pro894Ser | |
XM_011511688.1:c.1587-3351C>T | XP_011509990.1:n.1587-3351C>T | |
NM_001204.7:c.2680C>T MANE Select | NP_001195.2:p.Pro894Ser |