HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119326510_119326511del , CM000672.2:g.119326510_119326511del | GRCh38 |
NC_000010.10:g.121086022_121086023del , CM000672.1:g.121086022_121086023del | GRCh37 |
NC_000010.9:g.121076012_121076013del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000392870.3:c.53-6_53-5del MANE Select | ENSP00000376609.2:n.53-6_53-5del | |
ENST00000392870.2:c.53-6_53-5del | ENSP00000376609.2:n.53-6_53-5del | |
NM_005308.2:c.53-6_53-5del | NP_005299.1:n.53-6_53-5del | |
XM_005269707.1:c.53-6_53-5del | XP_005269764.1:n.53-6_53-5del | |
XM_005269708.1:c.53-54305_53-54304del | XP_005269765.1:n.53-54305_53-54304del | |
XM_005269707.2:c.53-6_53-5del | XP_005269764.1:n.53-6_53-5del | |
NM_005308.3:c.53-6_53-5del MANE Select | NP_005299.1:n.53-6_53-5del |