HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17024062C= , CM000663.2:g.17024062C= | GRCh38 |
NC_000001.10:g.17350557C= , CM000663.1:g.17350557C= | GRCh37 |
NC_000001.9:g.17223144C= | NCBI36 |
NG_012340.1:g.35109G= , LRG_316:g.35109G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.382G= | ENSP00000481376.2:p.Glu128= | |
ENST00000491274.6:c.511G= | ENSP00000480482.2:p.Glu171= | |
ENST00000375499.8:c.553G= MANE Select | ENSP00000364649.3:p.Glu185= | |
ENST00000375499.7:c.553G= | ENSP00000364649.3:p.Glu185= | |
ENST00000485515.5:n.487G= | ||
ENST00000491274.5:c.511G= | ENSP00000480482.1:p.Glu171= | |
NM_003000.2:c.553G= , LRG_316t1:c.553G= | NP_002991.2:p.Glu185= | |
NM_003000.3:c.553G= MANE Select | NP_002991.2:p.Glu185= |