HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2171793G= , CM000673.2:g.2171793G= | GRCh38 |
NC_000011.9:g.2193023G= , CM000673.1:g.2193023G= | GRCh37 |
NC_000011.8:g.2149599G= | NCBI36 |
NG_008128.1:g.5013C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000352909.8:c.-7C= MANE Select | ENSP00000325951.4:n.-7C= | |
ENST00000324155.8:c.-7C= | ENSP00000325831.3:n.-7C= | |
ENST00000333684.9:c.-7C= | ENSP00000328814.6:n.-7C= | |
ENST00000352909.7:c.-7C= | ENSP00000325951.3:n.-7C= | |
ENST00000381168.7:c.-7C= | ENSP00000370560.3:n.-7C= | |
ENST00000381175.5:c.-7C= | ENSP00000370567.1:n.-7C= | |
ENST00000381178.5:c.-7C= | ENSP00000370571.1:n.-7C= | |
NM_000360.3:c.-7C= | NP_000351.2:n.-7C= | |
NM_199292.2:c.-7C= | NP_954986.2:n.-7C= | |
NM_199293.2:c.-7C= | NP_954987.2:n.-7C= | |
XM_011520335.1:c.-7C= | XP_011518637.1:n.-7C= | |
XM_011520335.2:c.-7C= | XP_011518637.1:n.-7C= | |
NM_000360.4:c.-7C= MANE Select | NP_000351.2:n.-7C= | |
NM_199292.3:c.-7C= | NP_954986.2:n.-7C= | |
NM_199293.3:c.-7C= | NP_954987.2:n.-7C= |