HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21543244del , CM000669.2:g.21543244del | GRCh38 |
NC_000007.13:g.21582862del , CM000669.1:g.21582862del | GRCh37 |
NC_000007.12:g.21549387del | NCBI36 |
NG_012886.2:g.5030del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.-2del MANE Select | ENSP00000475939.1:n.-2del | |
ENST00000328843.10:c.-2del | ENSP00000330671.7:n.-2del | |
ENST00000409508.7:c.-2del | ENSP00000475939.1:n.-2del | |
ENST00000620169.4:c.-2del | ENSP00000481693.1:n.-2del | |
NM_001277115.1:c.-2del | NP_001264044.1:n.-2del | |
NM_001277115.2:c.-2del MANE Select | NP_001264044.1:n.-2del |