HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55063734T>A , CM000663.2:g.55063734T>A | GRCh38 |
NC_000001.10:g.55529407T>A , CM000663.1:g.55529407T>A | GRCh37 |
NC_000001.9:g.55301995T>A | NCBI36 |
NG_009061.1:g.29188T>A , LRG_275:g.29188T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.*569T>A | ENSP00000501161.2:n.*569T>A | |
ENST00000710286.1:c.*150T>A | ENSP00000518176.1:n.*150T>A | |
ENST00000673903.1:c.*150T>A | ENSP00000501257.1:n.*150T>A | |
ENST00000302118.5:c.*150T>A MANE Select | ENSP00000303208.5:n.*150T>A | |
ENST00000490692.1:n.2775T>A | ||
NM_174936.3:c.*150T>A , LRG_275t1:c.*150T>A | NP_777596.2:n.*150T>A | |
NR_110451.1:n.1836T>A | ||
XM_011541193.1:c.*150T>A | XP_011539495.1:n.*150T>A | |
NM_174936.4:c.*150T>A MANE Select | NP_777596.2:n.*150T>A | |
NR_110451.2:n.1836T>A |