HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240868837_240868838insA , CM000664.2:g.240868837_240868838insA | GRCh38 |
NC_000002.11:g.241808254_241808255insA , CM000664.1:g.241808254_241808255insA | GRCh37 |
NC_000002.10:g.241456927_241456928insA | NCBI36 |
NG_008005.1:g.5093_5094insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.-29_-28insA MANE Select | ENSP00000302620.3:n.-29_-28insA | |
ENST00000307503.3:c.-29_-28insA | ENSP00000302620.3:n.-29_-28insA | |
NM_000030.2:c.-29_-28insA | NP_000021.1:n.-29_-28insA | |
XR_924060.1:n.405+1395_405+1396insT | ||
NM_000030.3:c.-29_-28insA MANE Select | NP_000021.1:n.-29_-28insA |