HGVS | Genome Assembly |
---|---|
NC_000003.12:g.30606866C= , CM000665.2:g.30606866C= | GRCh38 |
NC_000003.11:g.30648358C= , CM000665.1:g.30648358C= | GRCh37 |
NC_000003.10:g.30623362C= | NCBI36 |
NG_007490.1:g.5365C= , LRG_779:g.5365C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000295754.10:c.-18C= MANE Select | ENSP00000295754.5:n.-18C= | |
ENST00000295754.9:c.-18C= | ENSP00000295754.5:n.-18C= | |
ENST00000359013.4:c.-18C= | ENSP00000351905.4:n.-18C= | |
NM_001024847.2:c.-18C= , LRG_779t1:c.-18C= | NP_001020018.1:n.-18C= | |
NM_003242.5:c.-18C= | NP_003233.4:n.-18C= | |
XM_011534045.1:c.-12+273C= | XP_011532347.1:n.-12+273C= | |
XM_011534045.3:c.-12+273C= | XP_011532347.1:n.-12+273C= | |
NM_003242.6:c.-18C= MANE Select | NP_003233.4:n.-18C= |