HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190408418G>C , CM000665.2:g.190408418G>C | GRCh38 |
NC_000003.11:g.190126207G>C , CM000665.1:g.190126207G>C | GRCh37 |
NC_000003.10:g.191608901G>C | NCBI36 |
NG_008149.1:g.25367G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264734.3:c.487G>C MANE Select | ENSP00000264734.3:p.Gly163Arg | |
ENST00000456423.2:c.115-1485G>C | ENSP00000414136.2:n.115-1485G>C | |
ENST00000264734.2:c.697G>C | ENSP00000264734.2:p.Gly233Arg | |
ENST00000456423.1:c.325-1485G>C | ENSP00000414136.1:n.325-1485G>C | |
NM_006580.3:c.697G>C | NP_006571.1:p.Gly233Arg | |
NM_001378492.1:c.487G>C | NP_001365421.1:p.Gly163Arg | |
NM_001378493.1:c.487G>C | NP_001365422.1:p.Gly163Arg | |
NM_006580.4:c.487G>C MANE Select | NP_006571.2:p.Gly163Arg |