HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240873200G= , CM000664.2:g.240873200G= | GRCh38 |
NC_000002.11:g.241812617G= , CM000664.1:g.241812617G= | GRCh37 |
NC_000002.10:g.241461290G= | NCBI36 |
NG_008005.1:g.9456G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.595+151G= MANE Select | ENSP00000302620.3:n.595+151G= | |
ENST00000307503.3:c.595+151G= | ENSP00000302620.3:n.595+151G= | |
ENST00000472436.1:n.766G= | ||
ENST00000476698.1:n.332+151G= | ||
NM_000030.2:c.595+151G= | NP_000021.1:n.595+151G= | |
NM_000030.3:c.595+151G= MANE Select | NP_000021.1:n.595+151G= |