HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55063859T>C , CM000663.2:g.55063859T>C | GRCh38 |
NC_000001.10:g.55529532T>C , CM000663.1:g.55529532T>C | GRCh37 |
NC_000001.9:g.55302120T>C | NCBI36 |
NG_009061.1:g.29313T>C , LRG_275:g.29313T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.*694T>C | ENSP00000501161.2:n.*694T>C | |
ENST00000710286.1:c.*275T>C | ENSP00000518176.1:n.*275T>C | |
ENST00000673903.1:c.*275T>C | ENSP00000501257.1:n.*275T>C | |
ENST00000302118.5:c.*275T>C MANE Select | ENSP00000303208.5:n.*275T>C | |
ENST00000490692.1:n.2900T>C | ||
NM_174936.3:c.*275T>C , LRG_275t1:c.*275T>C | NP_777596.2:n.*275T>C | |
NR_110451.1:n.1961T>C | ||
XM_011541193.1:c.*275T>C | XP_011539495.1:n.*275T>C | |
NM_174936.4:c.*275T>C MANE Select | NP_777596.2:n.*275T>C | |
NR_110451.2:n.1961T>C |