HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663119C>G , CM000676.2:g.36663119C>G | GRCh38 |
NC_000014.8:g.37132324C>G , CM000676.1:g.37132324C>G | GRCh37 |
NC_000014.7:g.36202075C>G | NCBI36 |
NG_013357.1:g.10552C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.227C>G MANE Select | ENSP00000355245.6:p.Pro76Arg | |
ENST00000555639.2:c.227C>G | ENSP00000501203.1:p.Pro76Arg | |
ENST00000361487.6:c.227C>G | ENSP00000355245.6:p.Pro76Arg | |
ENST00000402703.6:c.227C>G | ENSP00000384817.2:p.Pro76Arg | |
ENST00000554201.1:c.-335C>G | ENSP00000450434.1:n.-335C>G | |
ENST00000555639.1:n.529C>G | ||
NM_006194.3:c.227C>G | NP_006185.1:p.Pro76Arg | |
NM_001372076.1:c.227C>G MANE Select | NP_001359005.1:p.Pro76Arg | |
NM_006194.4:c.227C>G | NP_006185.1:p.Pro76Arg |