HGVS | Genome Assembly |
---|---|
NC_000015.10:g.38252926T>A , CM000677.2:g.38252926T>A | GRCh38 |
NC_000015.9:g.38545127T>A , CM000677.1:g.38545127T>A | GRCh37 |
NC_000015.8:g.36332419T>A | NCBI36 |
NG_008980.1:g.5076T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299084.9:c.-260T>A MANE Select | ENSP00000299084.4:n.-260T>A | |
ENST00000299084.8:c.-260T>A | ENSP00000299084.4:n.-260T>A | |
ENST00000561205.1:n.79T>A | ||
NM_152594.2:c.-260T>A | NP_689807.1:n.-260T>A | |
XM_005254202.2:c.-260T>A | XP_005254259.1:n.-260T>A | |
XM_005254203.3:c.-307T>A | XP_005254260.1:n.-307T>A | |
XM_005254202.3:c.-260T>A | XP_005254259.1:n.-260T>A | |
XR_001751484.1:n.87+641A>T | ||
NM_152594.3:c.-260T>A MANE Select | NP_689807.1:n.-260T>A |