HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188989632_188989637del , CM000664.2:g.188989632_188989637del | GRCh38 |
NC_000002.11:g.189854358_189854363del , CM000664.1:g.189854358_189854363del | GRCh37 |
NC_000002.10:g.189562603_189562608del | NCBI36 |
NG_007404.1:g.20260_20265del , LRG_3:g.20260_20265del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.690+183_690+188del | ENSP00000415346.2:n.690+183_690+188del | |
ENST00000304636.9:c.690+183_690+188del MANE Select | ENSP00000304408.4:n.690+183_690+188del | |
ENST00000304636.7:c.690+183_690+188del | ENSP00000304408.3:n.690+183_690+188del | |
ENST00000317840.9:c.690+183_690+188del | ENSP00000315243.6:n.690+183_690+188del | |
NM_000090.3:c.690+183_690+188del , LRG_3t1:c.690+183_690+188del | NP_000081.1:n.690+183_690+188del | |
NM_000090.4:c.690+183_690+188del MANE Select | NP_000081.2:n.690+183_690+188del |