HGVS | Genome Assembly |
---|---|
NC_000015.10:g.44711350T>G , CM000677.2:g.44711350T>G | GRCh38 |
NC_000015.9:g.45003548T>G , CM000677.1:g.45003548T>G | GRCh37 |
NC_000015.8:g.42790840T>G | NCBI36 |
NG_012920.1:g.4864T>G | |
NG_012920.2:g.4874T>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_011521338.1:c.-584A>C | XP_011519640.1:n.-584A>C | |
XM_011521339.1:c.-465A>C | XP_011519641.1:n.-465A>C | |
XM_011521340.1:c.-406A>C | XP_011519642.1:n.-406A>C | |
XM_011521343.1:c.-668A>C | XP_011519645.1:n.-668A>C | |
XM_011521345.1:c.-639A>C | XP_011519647.1:n.-639A>C | |
XM_011521338.3:c.-584A>C | XP_011519640.1:n.-584A>C | |
XM_011521339.3:c.-465A>C | XP_011519641.1:n.-465A>C | |
XM_011521340.3:c.-406A>C | XP_011519642.1:n.-406A>C | |
XM_011521343.3:c.-668A>C | XP_011519645.1:n.-668A>C | |
XM_011521345.3:c.-639A>C | XP_011519647.1:n.-639A>C | |
NM_001387260.1:c.-94A>C | NP_001374189.1:n.-94A>C |