HGVS | Genome Assembly |
---|---|
NC_000011.10:g.46894684A>C , CM000673.2:g.46894684A>C | GRCh38 |
NC_000011.9:g.46916235A>C , CM000673.1:g.46916235A>C | GRCh37 |
NC_000011.8:g.46872811A>C | NCBI36 |
NG_021394.1:g.28939T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378623.6:c.1445T>G MANE Select | ENSP00000367888.1:p.Val482Gly | |
ENST00000378623.5:c.1445T>G | ENSP00000367888.1:p.Val482Gly | |
NM_002334.3:c.1445T>G | NP_002325.2:p.Val482Gly | |
XM_011520102.1:c.1658T>G | XP_011518404.1:p.Val553Gly | |
XM_011520103.1:c.641T>G | XP_011518405.1:p.Val214Gly | |
XM_011520103.2:c.641T>G | XP_011518405.1:p.Val214Gly | |
XM_017017734.1:c.1445T>G | XP_016873223.1:p.Val482Gly | |
NM_002334.4:c.1445T>G MANE Select | NP_002325.2:p.Val482Gly |