HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189010787G= , CM000664.2:g.189010787G= | GRCh38 |
NC_000002.11:g.189875513G= , CM000664.1:g.189875513G= | GRCh37 |
NC_000002.10:g.189583758G= | NCBI36 |
NG_007404.1:g.41415G= , LRG_3:g.41415G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.4052G= | ENSP00000415346.2:p.Gly1351= | |
ENST00000304636.9:c.4151G= MANE Select | ENSP00000304408.4:p.Gly1384= | |
ENST00000304636.7:c.4151G= | ENSP00000304408.3:p.Gly1384= | |
ENST00000317840.9:c.3242G= | ENSP00000315243.6:p.Gly1081= | |
ENST00000487010.1:n.1530G= | ||
NM_000090.3:c.4151G= , LRG_3t1:c.4151G= | NP_000081.1:p.Gly1384= | |
NM_000090.4:c.4151G= MANE Select | NP_000081.2:p.Gly1384= |