HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4090336C= , CM000681.2:g.4090336C= | GRCh38 |
NC_000019.9:g.4090334C= , CM000681.1:g.4090334C= | GRCh37 |
NC_000019.8:g.4041334C= | NCBI36 |
NG_007996.1:g.38793G= , LRG_750:g.38793G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000689792.1:n.1369G= | ||
ENST00000262948.10:c.*262G= MANE Select | ENSP00000262948.4:n.*262G= | |
ENST00000262948.9:c.*262G= | ENSP00000262948.3:n.*262G= | |
ENST00000394867.8:c.*262G= | ENSP00000378336.1:n.*262G= | |
ENST00000600584.5:n.2914G= | ||
ENST00000601786.5:n.1766G= | ||
NM_030662.3:c.*262G= , LRG_750t1:c.*262G= | NP_109587.1:n.*262G= | |
XM_006722799.2:c.*262G= | XP_006722862.1:n.*262G= | |
XM_011528133.1:c.*262G= | XP_011526435.1:n.*262G= | |
NM_030662.4:c.*262G= MANE Select | NP_109587.1:n.*262G= |