HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129061513T>G , CM000665.2:g.129061513T>G | GRCh38 |
NC_000003.11:g.128780356T>G , CM000665.1:g.128780356T>G | GRCh37 |
NC_000003.10:g.130263046T>G | NCBI36 |
NG_008715.1:g.5712T>G , LRG_477:g.5712T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307395.5:c.-119T>G MANE Select | ENSP00000303942.4:n.-119T>G | |
ENST00000307395.4:c.-119T>G | ENSP00000303942.4:n.-119T>G | |
NM_000174.4:c.-119T>G , LRG_477t1:c.-119T>G | NP_000165.1:n.-119T>G | |
XM_005247374.3:c.-119T>G | XP_005247431.1:n.-119T>G | |
XM_011512701.1:c.-119T>G | XP_011511003.1:n.-119T>G | |
XM_011512702.1:c.-12-215T>G | XP_011511004.1:n.-12-215T>G | |
NM_000174.5:c.-119T>G MANE Select | NP_000165.1:n.-119T>G |