HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21043842C= , CM000664.2:g.21043842C= | GRCh38 |
NC_000002.11:g.21266714C= , CM000664.1:g.21266714C= | GRCh37 |
NC_000002.10:g.21120219C= | NCBI36 |
NG_011793.1:g.5232G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000673739.2:c.82+22G= | ENSP00000501110.2:n.82+22G= | |
ENST00000673882.2:c.82+22G= | ENSP00000501253.2:n.82+22G= | |
ENST00000233242.5:c.82+22G= MANE Select | ENSP00000233242.1:n.82+22G= | |
ENST00000399256.4:c.82+22G= | ENSP00000382200.4:n.82+22G= | |
ENST00000616098.4:c.82+22G= | ENSP00000477990.1:n.82+22G= | |
NM_000384.2:c.82+22G= | NP_000375.2:n.82+22G= | |
XM_011532809.1:c.82+22G= | XP_011531111.1:n.82+22G= | |
NM_000384.3:c.82+22G= MANE Select | NP_000375.3:n.82+22G= |