HGVS | Genome Assembly |
---|---|
NC_000014.9:g.20892108G>C , CM000676.2:g.20892108G>C | GRCh38 |
NC_000014.8:g.21360267G>C , CM000676.1:g.21360267G>C | GRCh37 |
NC_000014.7:g.20430107G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304639.4:c.422G>C MANE Select | ENSP00000302324.3:p.Arg141Thr | |
ENST00000304639.3:c.422G>C | ENSP00000302324.3:p.Arg141Thr | |
NM_002935.2:c.422G>C | NP_002926.2:p.Arg141Thr | |
XR_110261.2:n.209-16365C>G | ||
XR_110261.3:n.726-16365C>G | ||
NM_002935.3:c.422G>C MANE Select | NP_002926.2:p.Arg141Thr |