HGVS | Genome Assembly |
---|---|
NC_000023.11:g.106033604G>A , CM000685.2:g.106033604G>A | GRCh38 |
NC_000023.10:g.105277595G>A , CM000685.1:g.105277595G>A | GRCh37 |
NC_000023.9:g.105164251G>A | NCBI36 |
NG_021252.1:g.10124C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000372563.2:c.1144C>T MANE Select | ENSP00000361644.1:p.His382Tyr | |
ENST00000327674.8:c.1144C>T | ENSP00000329374.4:p.His382Tyr | |
ENST00000372563.1:c.1144C>T | ENSP00000361644.1:p.His382Tyr | |
NM_000354.5:c.1144C>T | NP_000345.2:p.His382Tyr | |
XM_006724683.1:c.1174C>T | XP_006724746.1:p.His392Tyr | |
XM_005262180.4:c.*89C>T | XP_005262237.1:n.*89C>T | |
XM_006724683.2:c.1174C>T | XP_006724746.1:p.His392Tyr | |
NM_000354.6:c.1144C>T MANE Select | NP_000345.2:p.His382Tyr |