HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31862023C= , CM000668.2:g.31862023C= | GRCh38 |
NC_000006.11:g.31829800C= , CM000668.1:g.31829800C= | GRCh37 |
NC_000006.10:g.31937779C= | NCBI36 |
NG_008201.1:g.5910G= | |
NG_023058.1:g.22024G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375631.5:c.328G= MANE Select | ENSP00000364782.4:p.Ala110= | |
ENST00000677054.1:n.457G= | ||
ENST00000677512.1:n.436G= | ||
ENST00000678869.1:n.436G= | ||
ENST00000375631.4:c.328G= | ENSP00000364782.4:p.Ala110= | |
ENST00000480384.1:n.357G= | ||
ENST00000491768.5:c.328G= | ENSP00000433127.1:p.Ala110= | |
ENST00000495807.1:n.348G= | ||
NM_000434.3:c.328G= | NP_000425.1:p.Ala110= | |
NM_000434.4:c.328G= MANE Select | NP_000425.1:p.Ala110= |