HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8015324C= , CM000679.2:g.8015324C= | GRCh38 |
NC_000017.10:g.7918642C= , CM000679.1:g.7918642C= | GRCh37 |
NC_000017.9:g.7859367C= | NCBI36 |
NG_009092.1:g.17655C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254854.5:c.2770-4C= MANE Select | ENSP00000254854.4:n.2770-4C= | |
ENST00000254854.4:c.2770-4C= | ENSP00000254854.4:n.2770-4C= | |
NM_000180.3:c.2770-4C= | NP_000171.1:n.2770-4C= | |
XM_011523816.1:c.2770-4C= | XP_011522118.1:n.2770-4C= | |
NM_000180.4:c.2770-4C= MANE Select | NP_000171.1:n.2770-4C= |