HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19954222G= , CM000670.2:g.19954222G= | GRCh38 |
NC_000008.10:g.19811733G= , CM000670.1:g.19811733G= | GRCh37 |
NC_000008.9:g.19856013G= | NCBI36 |
NG_008855.1:g.20152G= | |
NG_008855.2:g.57506G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.644G= MANE Select | ENSP00000497642.1:p.Gly215= | |
ENST00000311322.8:c.644G= | ENSP00000309757.6:p.Gly215= | |
NM_000237.2:c.644G= | NP_000228.1:p.Gly215= | |
NM_000237.3:c.644G= MANE Select | NP_000228.1:p.Gly215= |