HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443634_32443636delinsTTC , CM000668.2:g.32443634_32443636delinsTTC | GRCh38 |
NC_000006.11:g.32411411_32411413delinsTTC , CM000668.1:g.32411411_32411413delinsTTC | GRCh37 |
NC_000006.10:g.32519389_32519391delinsTTC | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000395388.7:c.611-122_611-120delinsTTC MANE Select | ENSP00000378786.2:n.611-122_611-120delinsTTC | |
ENST00000374982.5:c.536-122_536-120delinsTTC | ENSP00000364121.5:n.536-122_536-120delinsTTC | |
ENST00000395388.6:c.611-122_611-120delinsTTC | ENSP00000378786.2:n.611-122_611-120delinsTTC | |
NM_019111.4:c.611-122_611-120delinsTTC | NP_061984.2:n.611-122_611-120delinsTTC | |
NM_019111.5:c.611-122_611-120delinsTTC MANE Select | NP_061984.2:n.611-122_611-120delinsTTC |