HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750753T>A , CM000684.2:g.27750753T>A | GRCh38 |
NC_000022.10:g.28146741T>A , CM000684.1:g.28146741T>A | GRCh37 |
NC_000022.9:g.26476741T>A | NCBI36 |
NG_023258.1:g.55746A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703102.1:n.650A>T | ||
ENST00000302326.5:c.*162A>T MANE Select | ENSP00000304956.4:n.*162A>T | |
ENST00000302326.4:c.*162A>T | ENSP00000304956.4:n.*162A>T | |
ENST00000424656.1:c.455+23A>T | ||
ENST00000497225.1:n.481A>T | ||
NM_002430.2:c.*162A>T | NP_002421.3:n.*162A>T | |
NM_002430.3:c.*162A>T MANE Select | NP_002421.3:n.*162A>T |