HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31861159C= , CM000668.2:g.31861159C= | GRCh38 |
NC_000006.11:g.31828936C= , CM000668.1:g.31828936C= | GRCh37 |
NC_000006.10:g.31936915C= | NCBI36 |
NG_008201.1:g.6774G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375631.5:c.615+29G= MANE Select | ENSP00000364782.4:n.615+29G= | |
ENST00000677054.1:n.1321G= | ||
ENST00000677512.1:n.723+29G= | ||
ENST00000678869.1:n.752G= | ||
ENST00000375631.4:c.615+29G= | ENSP00000364782.4:n.615+29G= | |
ENST00000480384.1:n.644+29G= | ||
ENST00000491768.5:c.615+29G= | ENSP00000433127.1:n.615+29G= | |
ENST00000495807.1:n.1212G= | ||
NM_000434.3:c.615+29G= | NP_000425.1:n.615+29G= | |
NM_000434.4:c.615+29G= MANE Select | NP_000425.1:n.615+29G= |