HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4816252T>C , CM000681.2:g.4816252T>C | GRCh38 |
NC_000019.9:g.4816264T>C , CM000681.1:g.4816264T>C | GRCh37 |
NC_000019.8:g.4767264T>C | NCBI36 |
NG_031998.1:g.20491A>G , LRG_358:g.20491A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248244.6:c.2126A>G MANE Select | ENSP00000248244.4:p.Gln709Arg | |
ENST00000248244.5:c.2126A>G | ENSP00000248244.4:p.Gln709Arg | |
ENST00000621756.1:c.1628A>G | ENSP00000479467.1:p.Gln543Arg | |
NM_182919.3:c.2126A>G , LRG_358t1:c.2126A>G | NP_891549.1:p.Gln709Arg | |
NM_001385678.1:c.2084A>G | NP_001372607.1:p.Gln695Arg | |
NM_001385679.1:c.1991A>G | NP_001372608.1:p.Gln664Arg | |
NM_001385680.1:c.1484A>G | NP_001372609.1:p.Gln495Arg | |
NM_182919.4:c.2126A>G MANE Select | NP_891549.1:p.Gln709Arg |