HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49459061T= , CM000668.2:g.49459061T= | GRCh38 |
NC_000006.11:g.49426774T= , CM000668.1:g.49426774T= | GRCh37 |
NC_000006.10:g.49534733T= | NCBI36 |
NG_007100.1:g.9079A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.385+21A= MANE Select | ENSP00000274813.3:n.385+21A= | |
ENST00000274813.3:c.385+21A= | ENSP00000274813.3:n.385+21A= | |
NM_000255.3:c.385+21A= | NP_000246.2:n.385+21A= | |
XM_005249143.2:c.385+21A= | XP_005249200.1:n.385+21A= | |
XM_005249143.3:c.385+21A= | XP_005249200.1:n.385+21A= | |
NM_000255.4:c.385+21A= MANE Select | NP_000246.2:n.385+21A= |