HGVS | Genome Assembly |
---|---|
NC_000009.12:g.137139480C= , CM000671.2:g.137139480C= | GRCh38 |
NC_000009.11:g.140033932C= , CM000671.1:g.140033932C= | GRCh37 |
NC_000009.10:g.139153753C= | NCBI36 |
NG_011507.1:g.5324C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371553.8:c.-7C= | ENSP00000360608.3:n.-7C= | |
ENST00000371560.5:c.-7C= | ENSP00000360615.3:n.-7C= | |
ENST00000371561.8:c.-7C= MANE Select | ENSP00000360616.3:n.-7C= | |
ENST00000350902.9:c.-7C= | ENSP00000316915.9:n.-7C= | |
ENST00000371561.7:c.-7C= | ENSP00000360616.3:n.-7C= | |
ENST00000471122.5:n.71C= | ||
NM_000832.6:c.-7C= | NP_000823.4:n.-7C= | |
NM_001185090.1:c.-7C= | NP_001172019.1:n.-7C= | |
NM_001185091.1:c.-7C= | NP_001172020.1:n.-7C= | |
NM_007327.3:c.-7C= | NP_015566.1:n.-7C= | |
NM_021569.3:c.-7C= | NP_067544.1:n.-7C= | |
XM_005266071.2:c.-7C= | XP_005266128.1:n.-7C= | |
XM_005266072.2:c.-7C= | XP_005266129.1:n.-7C= | |
XM_005266073.3:c.-7C= | XP_005266130.1:n.-7C= | |
XM_011518583.1:c.-7C= | XP_011516885.1:n.-7C= | |
XM_005266072.3:c.-7C= | XP_005266129.1:n.-7C= | |
XM_005266073.4:c.-7C= | XP_005266130.1:n.-7C= | |
XM_011518583.2:c.-7C= | XP_011516885.1:n.-7C= | |
NM_007327.4:c.-7C= MANE Select | NP_015566.1:n.-7C= | |
NM_000832.7:c.-7C= | NP_000823.4:n.-7C= | |
NM_001185090.2:c.-7C= | NP_001172019.1:n.-7C= | |
NM_001185091.2:c.-7C= | NP_001172020.1:n.-7C= | |
NM_021569.4:c.-7C= | NP_067544.1:n.-7C= |