HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154957014T>C , CM000685.2:g.154957014T>C | GRCh38 |
NC_000023.10:g.154185289T>C , CM000685.1:g.154185289T>C | GRCh37 |
NC_000023.9:g.153838483T>C | NCBI36 |
NG_011403.1:g.70710A>G | |
NG_011403.2:g.70710A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.1695A>G MANE Select | ENSP00000353393.4:p.Gly565= | |
ENST00000647125.1:c.*1571A>G | ENSP00000496062.1:n.*1571A>G | |
ENST00000360256.8:c.1695A>G | ENSP00000353393.4:p.Gly565= | |
NM_000132.3:c.1695A>G | NP_000123.1:p.Gly565= | |
XM_011531126.1:c.1590A>G | XP_011529428.1:p.Gly530= | |
NM_000132.4:c.1695A>G MANE Select | NP_000123.1:p.Gly565= |