HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18223142A>C , CM000670.2:g.18223142A>C | GRCh38 |
NC_000008.10:g.18080651A>C , CM000670.1:g.18080651A>C | GRCh37 |
NC_000008.9:g.18124931A>C | NCBI36 |
NG_012245.2:g.57681A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307719.9:c.*222A>C MANE Select | ENSP00000307218.4:n.*222A>C | |
ENST00000545197.3:c.*222A>C | ENSP00000443194.1:n.*222A>C | |
ENST00000307719.8:c.*222A>C | ENSP00000307218.4:n.*222A>C | |
ENST00000517492.5:c.*222A>C | ENSP00000429407.1:n.*222A>C | |
ENST00000518029.5:c.*222A>C | ENSP00000428270.1:n.*222A>C | |
ENST00000520546.1:c.*222A>C | ENSP00000429341.1:n.*222A>C | |
ENST00000541942.1:c.*222A>C | ENSP00000440900.1:n.*222A>C | |
ENST00000545197.2:c.1281A>C | ENSP00000443194.1:n.1281A>C | |
NM_000662.7:c.*222A>C | NP_000653.3:n.*222A>C | |
NM_001160170.3:c.*222A>C | NP_001153642.1:n.*222A>C | |
NM_001160171.3:c.*222A>C | NP_001153643.1:n.*222A>C | |
NM_001160172.3:c.*222A>C | NP_001153644.1:n.*222A>C | |
NM_001160173.3:c.*222A>C | NP_001153645.1:n.*222A>C | |
NM_001160174.2:c.*222A>C | NP_001153646.1:n.*222A>C | |
NM_001160175.3:c.*222A>C | NP_001153647.1:n.*222A>C | |
NM_001160176.3:c.*222A>C | NP_001153648.1:n.*222A>C | |
NM_001160179.2:c.*222A>C | NP_001153651.1:n.*222A>C | |
NM_001291962.1:c.*222A>C | NP_001278891.1:n.*222A>C | |
XM_006716410.2:c.*222A>C | XP_006716473.1:n.*222A>C | |
XM_011544687.1:c.*222A>C | XP_011542989.1:n.*222A>C | |
XM_011544688.1:c.*222A>C | XP_011542990.1:n.*222A>C | |
XM_011544689.1:c.*222A>C | XP_011542991.1:n.*222A>C | |
XM_006716410.3:c.*222A>C | XP_006716473.1:n.*222A>C | |
XM_011544689.2:c.*222A>C | XP_011542991.1:n.*222A>C | |
XM_017013947.1:c.*222A>C | XP_016869436.1:n.*222A>C | |
NM_000662.8:c.*222A>C MANE Select | NP_000653.3:n.*222A>C | |
NM_001160170.4:c.*222A>C | NP_001153642.1:n.*222A>C | |
NM_001160171.4:c.*222A>C | NP_001153643.1:n.*222A>C | |
NM_001160172.4:c.*222A>C | NP_001153644.1:n.*222A>C | |
NM_001160175.4:c.*222A>C | NP_001153647.1:n.*222A>C | |
NM_001160176.4:c.*222A>C | NP_001153648.1:n.*222A>C | |
NM_001160179.3:c.*222A>C | NP_001153651.1:n.*222A>C | |
NM_001291962.2:c.*222A>C | NP_001278891.1:n.*222A>C | |
NM_001160173.4:c.*222A>C | NP_001153645.1:n.*222A>C | |
NM_001160174.3:c.*222A>C | NP_001153646.1:n.*222A>C |