HGVS | Genome Assembly |
---|---|
NC_000019.10:g.49636211_49636215del , CM000681.2:g.49636211_49636215del | GRCh38 |
NC_000019.9:g.50139468_50139472del , CM000681.1:g.50139468_50139472del | GRCh37 |
NC_000019.8:g.54831280_54831284del | NCBI36 |
NG_042222.1:g.8929_8933del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000246792.4:c.454-363_454-359del MANE Select | ENSP00000246792.2:n.454-363_454-359del | |
ENST00000246792.3:c.454-363_454-359del | ENSP00000246792.2:n.454-363_454-359del | |
ENST00000601532.1:n.594-363_594-359del | ||
NM_006270.3:c.454-363_454-359del | NP_006261.1:n.454-363_454-359del | |
NM_006270.4:c.454-363_454-359del | NP_006261.1:n.454-363_454-359del | |
NM_006270.5:c.454-363_454-359del MANE Select | NP_006261.1:n.454-363_454-359del |