HGVS | Genome Assembly |
---|---|
NC_000005.10:g.151259855C>G , CM000667.2:g.151259855C>G | GRCh38 |
NC_000005.9:g.150639416C>G , CM000667.1:g.150639416C>G | GRCh37 |
NC_000005.8:g.150619609C>G | NCBI36 |
NG_009059.1:g.11804C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357164.4:c.182C>G MANE Select | ENSP00000349687.3:p.Pro61Arg | |
ENST00000357164.3:c.182C>G | ENSP00000349687.3:p.Pro61Arg | |
ENST00000523004.1:c.57C>G | ||
ENST00000523466.5:c.227C>G | ENSP00000429100.1:p.Pro76Arg | |
NM_000405.4:c.182C>G | NP_000396.2:p.Pro61Arg | |
NM_001167607.1:c.182C>G | NP_001161079.1:p.Pro61Arg | |
NM_000405.5:c.182C>G MANE Select | NP_000396.2:p.Pro61Arg | |
NM_001167607.2:c.182C>G | NP_001161079.1:p.Pro61Arg | |
NM_001167607.3:c.182C>G | NP_001161079.1:p.Pro61Arg |