HGVS | Genome Assembly |
---|---|
NC_000012.12:g.68158740_68158743del , CM000674.2:g.68158740_68158743del | GRCh38 |
NC_000012.11:g.68552520_68552523del , CM000674.1:g.68552520_68552523del | GRCh37 |
NC_000012.10:g.66838787_66838790del | NCBI36 |
NG_015840.1:g.6024_6027del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000229135.4:c.115-459_115-456del MANE Select | ENSP00000229135.3:n.115-459_115-456del | |
ENST00000229135.3:c.115-459_115-456del | ENSP00000229135.3:n.115-459_115-456del | |
NM_000619.2:c.115-459_115-456del | NP_000610.2:n.115-459_115-456del | |
NM_000619.3:c.115-459_115-456del MANE Select | NP_000610.2:n.115-459_115-456del |