HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98186836_98186840del , CM000669.2:g.98186836_98186840del | GRCh38 |
NC_000007.13:g.97816148_97816152del , CM000669.1:g.97816148_97816152del | GRCh37 |
NC_000007.12:g.97654084_97654088del | NCBI36 |
NG_013375.1:g.84952_84956del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.877-41_877-37del MANE Select | ENSP00000297293.5:n.877-41_877-37del | |
ENST00000297293.5:c.877-41_877-37del | ENSP00000297293.5:n.877-41_877-37del | |
NM_014916.3:c.877-41_877-37del | NP_055731.2:n.877-41_877-37del | |
XM_011515981.1:c.871-41_871-37del | XP_011514283.1:n.871-41_871-37del | |
XM_011515981.3:c.871-41_871-37del | XP_011514283.1:n.871-41_871-37del | |
NM_014916.4:c.877-41_877-37del MANE Select | NP_055731.2:n.877-41_877-37del |