HGVS | Genome Assembly |
---|---|
NC_000004.12:g.69095621G>A , CM000666.2:g.69095621G>A | GRCh38 |
NC_000004.11:g.69961339G>A , CM000666.1:g.69961339G>A | GRCh37 |
NC_000004.10:g.69995928G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000502942.5:c.-26-2919G>A (UGT2B7) | ENSP00000426206.1:n.-26-2919G>A | |
ENST00000509763.1:n.260-2919G>A (UGT2B7) | ||
ENST00000615638.4:c.*106-90868C>T (UGT2B11) | ENSP00000477842.1:n.*106-90868C>T | |
ENST00000620779.4:c.*380-90868C>T (UGT2B11) | ENSP00000478182.1:n.*380-90868C>T | |
XM_005265702.2:c.-26-2919G>A (UGT2B7) | XP_005265759.1:n.-26-2919G>A | |
XM_011532231.1:c.-26-2919G>A (UGT2B7) | XP_011530533.1:n.-26-2919G>A | |
NM_001349568.1:c.-26-2919G>A (UGT2B7) | NP_001336497.1:n.-26-2919G>A | |
NM_001349568.2:c.-26-2919G>A (UGT2B7) | NP_001336497.1:n.-26-2919G>A |