HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154956968T>C , CM000685.2:g.154956968T>C | GRCh38 |
NC_000023.10:g.154185243T>C , CM000685.1:g.154185243T>C | GRCh37 |
NC_000023.9:g.153838437T>C | NCBI36 |
NG_011403.1:g.70756A>G | |
NG_011403.2:g.70756A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.1741A>G MANE Select | ENSP00000353393.4:p.Arg581Gly | |
ENST00000647125.1:c.*1617A>G | ENSP00000496062.1:n.*1617A>G | |
ENST00000360256.8:c.1741A>G | ENSP00000353393.4:p.Arg581Gly | |
NM_000132.3:c.1741A>G | NP_000123.1:p.Arg581Gly | |
XM_011531126.1:c.1636A>G | XP_011529428.1:p.Arg546Gly | |
NM_000132.4:c.1741A>G MANE Select | NP_000123.1:p.Arg581Gly |