HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119676693C>G , CM000672.2:g.119676693C>G | GRCh38 |
NC_000010.10:g.121436205C>G , CM000672.1:g.121436205C>G | GRCh37 |
NC_000010.9:g.121426195C>G | NCBI36 |
NG_016125.1:g.30324C>G , LRG_742:g.30324C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.1139C>G MANE Select | ENSP00000358081.4:p.Pro380Arg | |
ENST00000369085.7:c.1139C>G | ENSP00000358081.3:p.Pro380Arg | |
ENST00000450186.1:c.962C>G | ENSP00000410036.1:p.Pro321Arg | |
NM_004281.3:c.1139C>G , LRG_742t1:c.1139C>G | NP_004272.2:p.Pro380Arg | |
XM_005270287.1:c.1136C>G | XP_005270344.1:p.Pro379Arg | |
XM_005270287.2:c.1136C>G | XP_005270344.1:p.Pro379Arg | |
NM_004281.4:c.1139C>G MANE Select | NP_004272.2:p.Pro380Arg |