HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49459078_49459079insACCCTTA , CM000668.2:g.49459078_49459079insACCCTTA | GRCh38 |
NC_000006.11:g.49426791_49426792insACCCTTA , CM000668.1:g.49426791_49426792insACCCTTA | GRCh37 |
NC_000006.10:g.49534750_49534751insACCCTTA | NCBI36 |
NG_007100.1:g.9061_9062insTAAGGGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.385+3_385+4insTAAGGGT MANE Select | ENSP00000274813.3:n.385+3_385+4insTAAGGGT | |
ENST00000274813.3:c.385+3_385+4insTAAGGGT | ENSP00000274813.3:n.385+3_385+4insTAAGGGT | |
NM_000255.3:c.385+3_385+4insTAAGGGT | NP_000246.2:n.385+3_385+4insTAAGGGT | |
XM_005249143.2:c.385+3_385+4insTAAGGGT | XP_005249200.1:n.385+3_385+4insTAAGGGT | |
XM_005249143.3:c.385+3_385+4insTAAGGGT | XP_005249200.1:n.385+3_385+4insTAAGGGT | |
NM_000255.4:c.385+3_385+4insTAAGGGT MANE Select | NP_000246.2:n.385+3_385+4insTAAGGGT |