HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186194548C>G , CM000666.2:g.186194548C>G | GRCh38 |
NC_000004.11:g.187115702C>G , CM000666.1:g.187115702C>G | GRCh37 |
NC_000004.10:g.187352696C>G | NCBI36 |
NG_007965.1:g.8029C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.263C>G MANE Select | ENSP00000368079.4:p.Pro88Arg | |
ENST00000378802.4:c.263C>G | ENSP00000368079.4:p.Pro88Arg | |
NM_207352.3:c.263C>G | NP_997235.3:p.Pro88Arg | |
XM_005262935.2:c.263C>G | XP_005262992.1:p.Pro88Arg | |
XM_006714184.2:c.-48C>G | XP_006714247.1:n.-48C>G | |
XM_005262935.4:c.263C>G | XP_005262992.1:p.Pro88Arg | |
XM_017008037.1:c.-48C>G | XP_016863526.1:n.-48C>G | |
NM_207352.4:c.263C>G MANE Select | NP_997235.3:p.Pro88Arg |