HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750655C>A , CM000684.2:g.27750655C>A | GRCh38 |
NC_000022.10:g.28146643C>A , CM000684.1:g.28146643C>A | GRCh37 |
NC_000022.9:g.26476643C>A | NCBI36 |
NG_023258.1:g.55844G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703102.1:n.748G>T | ||
ENST00000302326.5:c.*260G>T MANE Select | ENSP00000304956.4:n.*260G>T | |
ENST00000302326.4:c.*260G>T | ENSP00000304956.4:n.*260G>T | |
ENST00000424656.1:c.455+121G>T | ||
NM_002430.2:c.*260G>T | NP_002421.3:n.*260G>T | |
NM_002430.3:c.*260G>T MANE Select | NP_002421.3:n.*260G>T |