HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94852467G= , CM000672.2:g.94852467G= | GRCh38 |
NC_000010.10:g.96612224G= , CM000672.1:g.96612224G= | GRCh37 |
NC_000010.9:g.96602214G= | NCBI36 |
NG_008384.2:g.94762G= | |
NG_008384.3:g.94787G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.1292-266G= MANE Select | ENSP00000360372.3:n.1292-266G= | |
ENST00000645461.1:n.2203-266G= | ||
ENST00000371321.7:c.1292-266G= | ENSP00000360372.3:n.1292-266G= | |
ENST00000464755.1:c.2055-266G= | ENSP00000483243.1:n.2055-266G= | |
NM_000769.2:c.1292-266G= | NP_000760.1:n.1292-266G= | |
NM_000769.4:c.1292-266G= MANE Select | NP_000760.1:n.1292-266G= |