HGVS | Genome Assembly |
---|---|
NC_000008.11:g.6877786_6877787insT , CM000670.2:g.6877786_6877787insT | GRCh38 |
NC_000008.10:g.6735308_6735309insT , CM000670.1:g.6735308_6735309insT | GRCh37 |
NC_000008.9:g.6722718_6722719insT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297439.4:c.61+10_61+11insA MANE Select | ENSP00000297439.3:n.61+10_61+11insA | |
ENST00000297439.3:c.61+10_61+11insA | ENSP00000297439.3:n.61+10_61+11insA | |
NM_005218.3:c.61+10_61+11insA | NP_005209.1:n.61+10_61+11insA | |
NM_005218.4:c.61+10_61+11insA MANE Select | NP_005209.1:n.61+10_61+11insA |