HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4816263C= , CM000681.2:g.4816263C= | GRCh38 |
NC_000019.9:g.4816275C= , CM000681.1:g.4816275C= | GRCh37 |
NC_000019.8:g.4767275C= | NCBI36 |
NG_031998.1:g.20480G= , LRG_358:g.20480G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248244.6:c.2115G= MANE Select | ENSP00000248244.4:p.Glu705= | |
ENST00000248244.5:c.2115G= | ENSP00000248244.4:p.Glu705= | |
ENST00000621756.1:c.1617G= | ENSP00000479467.1:p.Glu539= | |
NM_182919.3:c.2115G= , LRG_358t1:c.2115G= | NP_891549.1:p.Glu705= | |
NM_001385678.1:c.2073G= | NP_001372607.1:p.Glu691= | |
NM_001385679.1:c.1980G= | NP_001372608.1:p.Glu660= | |
NM_001385680.1:c.1473G= | NP_001372609.1:p.Glu491= | |
NM_182919.4:c.2115G= MANE Select | NP_891549.1:p.Glu705= |