HGVS | Genome Assembly |
---|---|
NC_000003.12:g.158644597C>T , CM000665.2:g.158644597C>T | GRCh38 |
NC_000003.11:g.158362386C>T , CM000665.1:g.158362386C>T | GRCh37 |
NC_000003.10:g.159845080C>T | NCBI36 |
NG_008441.1:g.5070C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000486715.6:c.-38C>T MANE Select | ENSP00000419038.1:n.-38C>T | |
ENST00000264263.9:c.-38C>T | ENSP00000264263.5:n.-38C>T | |
ENST00000478254.5:c.-38C>T | ENSP00000417225.1:n.-38C>T | |
ENST00000478576.5:c.-38C>T | ENSP00000418755.1:n.-38C>T | |
ENST00000486715.5:c.-38C>T | ENSP00000419038.1:n.-38C>T | |
NM_001308164.1:c.-38C>T | NP_001295093.1:n.-38C>T | |
NM_001308166.1:c.-38C>T | NP_001295095.1:n.-38C>T | |
NM_024996.5:c.-38C>T | NP_079272.4:n.-38C>T | |
XM_006713795.1:c.-38C>T | XP_006713858.1:n.-38C>T | |
XM_006713795.2:c.-38C>T | XP_006713858.1:n.-38C>T | |
NM_001374355.1:c.-38C>T | NP_001361284.1:n.-38C>T | |
NM_001374356.1:c.-38C>T | NP_001361285.1:n.-38C>T | |
NM_001374357.1:c.-429C>T | NP_001361286.1:n.-429C>T | |
NM_001374358.1:c.-38C>T | NP_001361287.1:n.-38C>T | |
NM_001374359.1:c.-267C>T | NP_001361288.1:n.-267C>T | |
NM_001374360.1:c.-267C>T | NP_001361289.1:n.-267C>T | |
NM_001374361.1:c.-267C>T | NP_001361290.1:n.-267C>T | |
NM_024996.7:c.-38C>T MANE Select | NP_079272.4:n.-38C>T | |
NR_164499.1:n.71C>T | ||
NR_164500.1:n.71C>T | ||
NR_164501.1:n.71C>T | ||
NR_164502.1:n.71C>T | ||
NM_001308164.2:c.-38C>T | NP_001295093.1:n.-38C>T | |
NM_001308166.2:c.-38C>T | NP_001295095.1:n.-38C>T |