HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98186863_98186866del , CM000669.2:g.98186863_98186866del | GRCh38 |
NC_000007.13:g.97816175_97816178del , CM000669.1:g.97816175_97816178del | GRCh37 |
NC_000007.12:g.97654111_97654114del | NCBI36 |
NG_013375.1:g.84979_84982del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.877-14_877-11del MANE Select | ENSP00000297293.5:n.877-14_877-11del | |
ENST00000297293.5:c.877-14_877-11del | ENSP00000297293.5:n.877-14_877-11del | |
NM_014916.3:c.877-14_877-11del | NP_055731.2:n.877-14_877-11del | |
XM_011515981.1:c.871-14_871-11del | XP_011514283.1:n.871-14_871-11del | |
XM_011515981.3:c.871-14_871-11del | XP_011514283.1:n.871-14_871-11del | |
NM_014916.4:c.877-14_877-11del MANE Select | NP_055731.2:n.877-14_877-11del |