HGVS | Genome Assembly |
---|---|
NC_000009.12:g.130452226G= , CM000671.2:g.130452226G= | GRCh38 |
NC_000009.11:g.133327613G= , CM000671.1:g.133327613G= | GRCh37 |
NC_000009.10:g.132317434G= | NCBI36 |
NG_011542.1:g.12520G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000352480.10:c.-3G= MANE Select | ENSP00000253004.6:n.-3G= | |
ENST00000352480.9:c.-3G= | ENSP00000253004.6:n.-3G= | |
ENST00000372393.7:c.-3G= | ENSP00000361469.2:n.-3G= | |
ENST00000372394.5:c.-3G= | ENSP00000361471.1:n.-3G= | |
ENST00000422569.5:c.-3G= | ENSP00000394212.1:n.-3G= | |
ENST00000443588.1:c.-3G= | ENSP00000397785.1:n.-3G= | |
NM_000050.4:c.-3G= | NP_000041.2:n.-3G= | |
NM_054012.3:c.-3G= | NP_446464.1:n.-3G= | |
XM_005272200.2:c.-3G= | XP_005272257.1:n.-3G= | |
XM_011518705.1:c.112G= | XP_011517007.1:p.Ala38= | |
XM_005272200.3:c.-3G= | XP_005272257.1:n.-3G= | |
XM_011518705.2:c.112G= | XP_011517007.1:p.Ala38= | |
XM_017014729.1:c.94G= | XP_016870218.1:p.Ala32= | |
NM_054012.4:c.-3G= MANE Select | NP_446464.1:n.-3G= |