HGVS | Genome Assembly |
---|---|
NC_000001.11:g.41479027G>A , CM000663.2:g.41479027G>A | GRCh38 |
NC_000001.10:g.41944698G>A , CM000663.1:g.41944698G>A | GRCh37 |
NC_000001.9:g.41717285G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372587.5:c.*382C>T MANE Select | ENSP00000361668.4:n.*382C>T | |
ENST00000372587.4:c.*382C>T | ENSP00000361668.4:n.*382C>T | |
NM_001302269.1:c.*382C>T | NP_001289198.1:n.*382C>T | |
NM_001956.4:c.*382C>T | NP_001947.1:n.*382C>T | |
NR_126098.1:n.910C>T | ||
XM_017000512.1:c.*382C>T | XP_016856001.1:n.*382C>T | |
NM_001956.5:c.*382C>T MANE Select | NP_001947.1:n.*382C>T | |
NM_001302269.2:c.*382C>T | NP_001289198.1:n.*382C>T | |
NR_126098.2:n.910C>T |