HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154569395G= , CM000663.2:g.154569395G= | GRCh38 |
NC_000001.10:g.154541871G= , CM000663.1:g.154541871G= | GRCh37 |
NC_000001.9:g.152808495G= | NCBI36 |
NG_008027.1:g.6615G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368476.4:c.65-67G= MANE Select | ENSP00000357461.3:n.65-67G= | |
ENST00000636034.1:c.65-67G= | ENSP00000489703.1:n.65-67G= | |
ENST00000637900.1:c.65-67G= | ENSP00000490474.1:n.65-67G= | |
ENST00000368476.3:c.65-67G= | ENSP00000357461.3:n.65-67G= | |
NM_000748.2:c.65-67G= | NP_000739.1:n.65-67G= | |
XM_017000180.2:c.-310-67G= | XP_016855669.1:n.-310-67G= | |
XR_001736952.2:n.317-67G= | ||
NM_000748.3:c.65-67G= MANE Select | NP_000739.1:n.65-67G= |