HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98186856G>A , CM000669.2:g.98186856G>A | GRCh38 |
NC_000007.13:g.97816168G>A , CM000669.1:g.97816168G>A | GRCh37 |
NC_000007.12:g.97654104G>A | NCBI36 |
NG_013375.1:g.84972G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297293.6:c.877-21G>A MANE Select | ENSP00000297293.5:n.877-21G>A | |
ENST00000297293.5:c.877-21G>A | ENSP00000297293.5:n.877-21G>A | |
NM_014916.3:c.877-21G>A | NP_055731.2:n.877-21G>A | |
XM_011515981.1:c.871-21G>A | XP_011514283.1:n.871-21G>A | |
XM_011515981.3:c.871-21G>A | XP_011514283.1:n.871-21G>A | |
NM_014916.4:c.877-21G>A MANE Select | NP_055731.2:n.877-21G>A |