HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48459706T>G , CM000675.2:g.48459706T>G | GRCh38 |
NC_000013.10:g.49033842T>G , CM000675.1:g.49033842T>G | GRCh37 |
NC_000013.9:g.47931843T>G | NCBI36 |
NG_009009.1:g.160960T>G , LRG_517:g.160960T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.1979T>G MANE Select | ENSP00000267163.4:p.Leu660Arg | |
ENST00000643064.1:c.194+78263T>G | ||
ENST00000650461.1:c.1979T>G | ENSP00000497193.1:p.Leu660Arg | |
ENST00000267163.4:c.1979T>G | ENSP00000267163.4:p.Leu660Arg | |
NM_000321.2:c.1979T>G , LRG_517t1:c.1979T>G | NP_000312.2:p.Leu660Arg | |
XM_011535171.1:c.1718T>G | XP_011533473.1:p.Leu573Arg | |
XM_011535171.2:c.1718T>G | XP_011533473.1:p.Leu573Arg | |
NM_000321.3:c.1979T>G MANE Select | NP_000312.2:p.Leu660Arg |