HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18787640G>C , CM000681.2:g.18787640G>C | GRCh38 |
NC_000019.9:g.18898449G>C , CM000681.1:g.18898449G>C | GRCh37 |
NC_000019.8:g.18759449G>C | NCBI36 |
NG_007070.1:g.8666C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.986C>G MANE Select | ENSP00000222271.2:p.Pro329Arg | |
ENST00000222271.6:c.986C>G | ENSP00000222271.2:p.Pro329Arg | |
ENST00000425807.1:c.827C>G | ENSP00000403792.1:p.Pro276Arg | |
ENST00000542601.6:c.887C>G | ENSP00000439156.2:p.Pro296Arg | |
NM_000095.2:c.986C>G | NP_000086.2:p.Pro329Arg | |
NM_000095.3:c.986C>G MANE Select | NP_000086.2:p.Pro329Arg |