HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15180569C= , CM000681.2:g.15180569C= | GRCh38 |
NC_000019.9:g.15291380C= , CM000681.1:g.15291380C= | GRCh37 |
NC_000019.8:g.15152380C= | NCBI36 |
NG_009819.1:g.25413G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.3142+112G= MANE Select | ENSP00000263388.1:n.3142+112G= | |
ENST00000263388.6:c.3142+112G= | ENSP00000263388.1:n.3142+112G= | |
ENST00000601011.1:c.2983+112G= | ENSP00000473138.1:n.2983+112G= | |
NM_000435.2:c.3142+112G= | NP_000426.2:n.3142+112G= | |
XM_005259924.3:c.2986+112G= | XP_005259981.1:n.2986+112G= | |
XM_005259924.4:c.2986+112G= | XP_005259981.1:n.2986+112G= | |
NM_000435.3:c.3142+112G= MANE Select | NP_000426.2:n.3142+112G= |