HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31859945C>A , CM000668.2:g.31859945C>A | GRCh38 |
NC_000006.11:g.31827722C>A , CM000668.1:g.31827722C>A | GRCh37 |
NC_000006.10:g.31935701C>A | NCBI36 |
NG_008201.1:g.7988G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375631.5:c.1022G>T MANE Select | ENSP00000364782.4:p.Arg341Leu | |
ENST00000677054.1:n.2361G>T | ||
ENST00000677512.1:n.1299G>T | ||
ENST00000678869.1:n.1610G>T | ||
ENST00000375631.4:c.1022G>T | ENSP00000364782.4:p.Arg341Leu | |
ENST00000480384.1:n.1321G>T | ||
ENST00000491768.5:c.*132G>T | ENSP00000433127.1:n.*132G>T | |
ENST00000495807.1:n.2330G>T | ||
NM_000434.3:c.1022G>T | NP_000425.1:p.Arg341Leu | |
NM_000434.4:c.1022G>T MANE Select | NP_000425.1:p.Arg341Leu |