HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67940828_67940833del , CM000678.2:g.67940828_67940833del | GRCh38 |
NC_000016.9:g.67974731_67974736del , CM000678.1:g.67974731_67974736del | GRCh37 |
NC_000016.8:g.66532232_66532237del | NCBI36 |
NG_009778.1:g.8282_8287del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264005.10:c.749-353_749-348del MANE Select | ENSP00000264005.5:n.749-353_749-348del | |
ENST00000264005.9:c.749-353_749-348del | ENSP00000264005.5:n.749-353_749-348del | |
ENST00000570369.5:c.156-757_156-752del | ||
ENST00000570980.1:c.533-353_533-348del | ENSP00000464651.1:n.533-353_533-348del | |
ENST00000573538.5:c.392_397del | ||
NM_000229.1:c.749-353_749-348del | NP_000220.1:n.749-353_749-348del | |
NM_000229.2:c.749-353_749-348del MANE Select | NP_000220.1:n.749-353_749-348del |