HGVS | Genome Assembly |
---|---|
NC_000002.12:g.32063825G= , CM000664.2:g.32063825G= | GRCh38 |
NC_000002.11:g.32288894G= , CM000664.1:g.32288894G= | GRCh37 |
NC_000002.10:g.32142398G= | NCBI36 |
NG_008730.1:g.5215G= , LRG_714:g.5215G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000704289.1:c.-7G= | ENSP00000515816.1:n.-7G= | |
ENST00000315285.9:c.-7G= MANE Select | ENSP00000320885.3:n.-7G= | |
ENST00000621856.2:c.-7G= | ENSP00000482496.2:n.-7G= | |
ENST00000646571.1:c.-7G= | ENSP00000495015.1:n.-7G= | |
ENST00000315285.7:c.-7G= | ENSP00000320885.3:n.-7G= | |
ENST00000345662.5:c.-7G= | ENSP00000340817.1:n.-7G= | |
ENST00000615843.4:c.-7G= | ENSP00000480893.1:n.-7G= | |
NM_014946.3:c.-7G= , LRG_714t1:c.-7G= | NP_055761.2:n.-7G= | |
NM_199436.1:c.-7G= | NP_955468.1:n.-7G= | |
XM_005264516.3:c.-7G= | XP_005264573.1:n.-7G= | |
XM_011533067.1:c.-7G= | XP_011531369.1:n.-7G= | |
NM_001363823.1:c.-7G= | NP_001350752.1:n.-7G= | |
NM_001363875.1:c.-7G= | NP_001350804.1:n.-7G= | |
XM_011533067.2:c.-7G= | XP_011531369.1:n.-7G= | |
XM_017004778.2:c.-7G= | XP_016860267.1:n.-7G= | |
NM_001363823.2:c.-7G= | NP_001350752.1:n.-7G= | |
NM_001363875.2:c.-7G= | NP_001350804.1:n.-7G= | |
NM_001377959.1:c.-7G= | NP_001364888.1:n.-7G= | |
NM_014946.4:c.-7G= MANE Select | NP_055761.2:n.-7G= | |
NM_199436.2:c.-7G= | NP_955468.1:n.-7G= |