HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189062929A>G , CM000664.2:g.189062929A>G | GRCh38 |
NC_000002.11:g.189927655A>G , CM000664.1:g.189927655A>G | GRCh37 |
NC_000002.10:g.189635900A>G | NCBI36 |
NG_011799.1:g.121951T>C | |
NG_011799.2:g.121951T>C | |
NG_011799.3:g.167373T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.1924-11T>C MANE Select | ENSP00000364000.3:n.1924-11T>C | |
ENST00000374866.7:c.1924-11T>C | ENSP00000364000.3:n.1924-11T>C | |
ENST00000470524.2:n.30-11T>C | ||
ENST00000618828.1:c.763-11T>C | ENSP00000482184.1:n.763-11T>C | |
NM_000393.3:c.1924-11T>C | NP_000384.2:n.1924-11T>C | |
XM_011510573.1:c.1786-11T>C | XP_011508875.1:n.1786-11T>C | |
NM_000393.4:c.1924-11T>C | NP_000384.2:n.1924-11T>C | |
XM_011510573.3:c.1786-11T>C | XP_011508875.1:n.1786-11T>C | |
NM_000393.5:c.1924-11T>C MANE Select | NP_000384.2:n.1924-11T>C |