HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18787517G= , CM000681.2:g.18787517G= | GRCh38 |
NC_000019.9:g.18898326G= , CM000681.1:g.18898326G= | GRCh37 |
NC_000019.8:g.18759326G= | NCBI36 |
NG_007070.1:g.8789C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.1109C= MANE Select | ENSP00000222271.2:p.Ala370= | |
ENST00000222271.6:c.1109C= | ENSP00000222271.2:p.Ala370= | |
ENST00000425807.1:c.950C= | ENSP00000403792.1:p.Ala317= | |
ENST00000542601.6:c.1010C= | ENSP00000439156.2:p.Ala337= | |
NM_000095.2:c.1109C= | NP_000086.2:p.Ala370= | |
NM_000095.3:c.1109C= MANE Select | NP_000086.2:p.Ala370= |