HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134375551_134375552del , CM000671.2:g.134375551_134375552del | GRCh38 |
NC_000009.11:g.137267397_137267398del , CM000671.1:g.137267397_137267398del | GRCh37 |
NC_000009.10:g.136407218_136407219del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000481739.2:c.29-26081_29-26080del MANE Select | ENSP00000419692.1:n.29-26081_29-26080del | |
ENST00000356384.4:n.293+1421_293+1422del | ||
ENST00000481739.1:c.29-26081_29-26080del | ENSP00000419692.1:n.29-26081_29-26080del | |
ENST00000484822.1:n.453-26081_453-26080del | ||
NM_002957.5:c.29-26081_29-26080del | NP_002948.1:n.29-26081_29-26080del | |
NM_002957.6:c.29-26081_29-26080del MANE Select | NP_002948.1:n.29-26081_29-26080del |