HGVS | Genome Assembly |
---|---|
NC_000023.11:g.151403709A>G , CM000685.2:g.151403709A>G | GRCh38 |
NC_000023.10:g.150572181A>G , CM000685.1:g.150572181A>G | GRCh37 |
NC_000023.9:g.150322839A>G | NCBI36 |
NG_016761.1:g.11525A>G , LRG_860:g.11525A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330374.7:c.132A>G MANE Select | ENSP00000333255.6:p.Leu44= | |
ENST00000330374.6:c.132A>G | ENSP00000333255.6:p.Leu44= | |
ENST00000370361.5:c.297A>G | ENSP00000359386.1:p.Leu99= | |
ENST00000477649.1:n.212A>G | ||
NM_001017980.3:c.132A>G , LRG_860t1:c.132A>G | NP_001017980.1:p.Leu44= | |
XM_011531125.1:c.297A>G | XP_011529427.1:p.Leu99= | |
NM_001363810.1:c.297A>G | NP_001350739.1:p.Leu99= | |
NM_001017980.4:c.132A>G MANE Select | NP_001017980.1:p.Leu44= |