HGVS | Genome Assembly |
---|---|
NC_000007.14:g.92496713del , CM000669.2:g.92496713del | GRCh38 |
NC_000007.13:g.92126027del , CM000669.1:g.92126027del | GRCh37 |
NC_000007.12:g.91963963del | NCBI36 |
NG_008341.1:g.36820del | |
NG_008341.2:g.36820del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000248633.9:c.2783+1del | ||
ENST00000248633.8:c.2783+1del | ||
ENST00000428214.5:c.2612+1del | ||
ENST00000438045.5:c.1817+1del | ||
ENST00000484913.5:n.2822+1del | ||
ENST00000496420.5:n.2675+1del | ||
NM_000466.2:c.2783+1del | ||
NM_001282677.1:c.2612+1del | ||
NM_001282678.1:c.2159+1del | ||
XM_005250433.3:c.1034+1del | ||
XR_242246.3:n.2879+1del | ||
XM_017012319.2:c.1034+1del | ||
XR_001744808.2:n.1810+1del | ||
XR_242246.5:n.2830+1del | ||
NM_000466.3:c.2783+1del | ||
NM_001282677.2:c.2612+1del | ||
NM_001282678.2:c.2159+1del |