HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98187062_98187063insGA , CM000669.2:g.98187062_98187063insGA | GRCh38 |
NC_000007.13:g.97816374_97816375insGA , CM000669.1:g.97816374_97816375insGA | GRCh37 |
NC_000007.12:g.97654310_97654311insGA | NCBI36 |
NG_013375.1:g.85178_85179insGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.998+64_998+65insGA MANE Select | ENSP00000297293.5:n.998+64_998+65insGA | |
ENST00000297293.5:c.998+64_998+65insGA | ENSP00000297293.5:n.998+64_998+65insGA | |
NM_014916.3:c.998+64_998+65insGA | NP_055731.2:n.998+64_998+65insGA | |
XM_011515981.1:c.992+64_992+65insGA | XP_011514283.1:n.992+64_992+65insGA | |
XM_011515981.3:c.992+64_992+65insGA | XP_011514283.1:n.992+64_992+65insGA | |
NM_014916.4:c.998+64_998+65insGA MANE Select | NP_055731.2:n.998+64_998+65insGA |