HGVS | Genome Assembly |
---|---|
NC_000009.12:g.98542021G>C , CM000671.2:g.98542021G>C | GRCh38 |
NC_000009.11:g.101304303G>C , CM000671.1:g.101304303G>C | GRCh37 |
NC_000009.10:g.100344124G>C | NCBI36 |
NG_016426.1:g.172177C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259455.4:c.482C>G MANE Select | ENSP00000259455.2:p.Pro161Arg | |
ENST00000637410.1:n.260C>G | ||
ENST00000637717.1:c.98C>G | ENSP00000490789.1:p.Pro33Arg | |
ENST00000638001.1:n.92C>G | ||
ENST00000259455.3:c.482C>G | ENSP00000259455.2:p.Pro161Arg | |
ENST00000477471.1:n.269C>G | ||
ENST00000634227.1:n.256C>G | ||
NM_005458.7:c.482C>G | NP_005449.5:p.Pro161Arg | |
XM_017015331.2:c.188C>G | XP_016870820.1:p.Pro63Arg | |
NM_005458.8:c.482C>G MANE Select | NP_005449.5:p.Pro161Arg |