HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240869089_240869092del , CM000664.2:g.240869089_240869092del | GRCh38 |
NC_000002.11:g.241808506_241808509del , CM000664.1:g.241808506_241808509del | GRCh37 |
NC_000002.10:g.241457179_241457182del | NCBI36 |
NG_008005.1:g.5345_5348del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.165+59_165+62del MANE Select | ENSP00000302620.3:n.165+59_165+62del | |
ENST00000307503.3:c.165+59_165+62del | ENSP00000302620.3:n.165+59_165+62del | |
ENST00000472436.1:n.185+59_185+62del | ||
NM_000030.2:c.165+59_165+62del | NP_000021.1:n.165+59_165+62del | |
XR_924060.1:n.405+1141_405+1144del | ||
NM_000030.3:c.165+59_165+62del MANE Select | NP_000021.1:n.165+59_165+62del |