HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98186840T= , CM000669.2:g.98186840T= | GRCh38 |
NC_000007.13:g.97816152T= , CM000669.1:g.97816152T= | GRCh37 |
NC_000007.12:g.97654088T= | NCBI36 |
NG_013375.1:g.84956T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.877-37T= MANE Select | ENSP00000297293.5:n.877-37T= | |
ENST00000297293.5:c.877-37T= | ENSP00000297293.5:n.877-37T= | |
NM_014916.3:c.877-37T= | NP_055731.2:n.877-37T= | |
XM_011515981.1:c.871-37T= | XP_011514283.1:n.871-37T= | |
XM_011515981.3:c.871-37T= | XP_011514283.1:n.871-37T= | |
NM_014916.4:c.877-37T= MANE Select | NP_055731.2:n.877-37T= |