HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154957053G>C , CM000685.2:g.154957053G>C | GRCh38 |
NC_000023.10:g.154185328G>C , CM000685.1:g.154185328G>C | GRCh37 |
NC_000023.9:g.153838522G>C | NCBI36 |
NG_011403.1:g.70671C>G | |
NG_011403.2:g.70671C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.1656C>G MANE Select | ENSP00000353393.4:p.Tyr552Ter | |
ENST00000647125.1:c.*1532C>G | ENSP00000496062.1:n.*1532C>G | |
ENST00000360256.8:c.1656C>G | ENSP00000353393.4:p.Tyr552Ter | |
NM_000132.3:c.1656C>G | NP_000123.1:p.Tyr552Ter | |
XM_011531126.1:c.1551C>G | XP_011529428.1:p.Tyr517Ter | |
NM_000132.4:c.1656C>G MANE Select | NP_000123.1:p.Tyr552Ter |