HGVS | Genome Assembly |
---|---|
NC_000012.12:g.51920894C= , CM000674.2:g.51920894C= | GRCh38 |
NC_000012.11:g.52314678C= , CM000674.1:g.52314678C= | GRCh37 |
NC_000012.10:g.50600945C= | NCBI36 |
NG_009549.1:g.18477C= , LRG_543:g.18477C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000551576.6:c.*1C= | ENSP00000455848.2:n.*1C= | |
ENST00000388922.9:c.*1C= MANE Select | ENSP00000373574.4:n.*1C= | |
ENST00000388922.8:c.*1C= | ENSP00000373574.4:n.*1C= | |
ENST00000419526.6:c.*1C= | ENSP00000392492.2:n.*1C= | |
ENST00000550683.5:c.*1C= | ENSP00000447884.1:n.*1C= | |
NM_000020.2:c.*1C= , LRG_543t1:c.*1C= | NP_000011.2:n.*1C= | |
NM_001077401.1:c.*1C= | NP_001070869.1:n.*1C= | |
XM_005269235.2:c.*1C= | XP_005269292.1:n.*1C= | |
XM_011539008.1:c.*1C= | XP_011537310.1:n.*1C= | |
XM_024449279.1:c.*1C= | XP_024305047.1:n.*1C= | |
NM_000020.3:c.*1C= MANE Select | NP_000011.2:n.*1C= | |
NM_001077401.2:c.*1C= | NP_001070869.1:n.*1C= |