HGVS | Genome Assembly |
---|---|
NC_000001.11:g.41479035A>G , CM000663.2:g.41479035A>G | GRCh38 |
NC_000001.10:g.41944706A>G , CM000663.1:g.41944706A>G | GRCh37 |
NC_000001.9:g.41717293A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372587.5:c.*374T>C MANE Select | ENSP00000361668.4:n.*374T>C | |
ENST00000372587.4:c.*374T>C | ENSP00000361668.4:n.*374T>C | |
NM_001302269.1:c.*374T>C | NP_001289198.1:n.*374T>C | |
NM_001956.4:c.*374T>C | NP_001947.1:n.*374T>C | |
NR_126098.1:n.902T>C | ||
XM_017000512.1:c.*374T>C | XP_016856001.1:n.*374T>C | |
NM_001956.5:c.*374T>C MANE Select | NP_001947.1:n.*374T>C | |
NM_001302269.2:c.*374T>C | NP_001289198.1:n.*374T>C | |
NR_126098.2:n.902T>C |