HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431192_23431193del , CM000676.2:g.23431192_23431193del | GRCh38 |
NC_000014.8:g.23900401_23900402del , CM000676.1:g.23900401_23900402del | GRCh37 |
NC_000014.7:g.22970241_22970242del | NCBI36 |
NG_007884.1:g.9470_9471del , LRG_384:g.9470_9471del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.797-193_797-192del MANE Select | ENSP00000347507.3:n.797-193_797-192del | |
ENST00000355349.3:c.797-193_797-192del | ENSP00000347507.3:n.797-193_797-192del | |
NM_000257.3:c.797-193_797-192del | NP_000248.2:n.797-193_797-192del | |
XR_245686.3:n.903-193_903-192del | ||
XM_017021340.1:c.797-193_797-192del | XP_016876829.1:n.797-193_797-192del | |
NM_000257.4:c.797-193_797-192del MANE Select | NP_000248.2:n.797-193_797-192del |