HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1013951G= , CM000663.2:g.1013951G= | GRCh38 |
NC_000001.10:g.949331G= , CM000663.1:g.949331G= | GRCh37 |
NC_000001.9:g.939194G= | NCBI36 |
NG_033033.1:g.5485G= | |
NG_033033.2:g.17814G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624697.4:c.-21-33G= | ENSP00000485643.1:n.-21-33G= | |
ENST00000649529.1:c.4-33G= MANE Select | ENSP00000496832.1:n.4-33G= | |
ENST00000379389.4:c.4-33G= | ENSP00000368699.4:n.4-33G= | |
ENST00000624652.1:c.-21-33G= | ENSP00000485313.1:n.-21-33G= | |
ENST00000624697.3:c.-21-33G= | ENSP00000485643.1:n.-21-33G= | |
NM_005101.3:c.4-33G= | NP_005092.1:n.4-33G= | |
NM_005101.4:c.4-33G= MANE Select | NP_005092.1:n.4-33G= |