HGVS | Genome Assembly |
---|---|
NC_000002.12:g.137118294G>T , CM000664.2:g.137118294G>T | GRCh38 |
NC_000002.11:g.137875864G>T , CM000664.1:g.137875864G>T | GRCh37 |
NC_000002.10:g.137592334G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409968.6:c.1369+3001G>T MANE Select | ENSP00000387145.1:n.1369+3001G>T | |
ENST00000272643.7:c.1369+3001G>T | ENSP00000272643.4:n.1369+3001G>T | |
ENST00000409968.5:c.1369+3001G>T | ENSP00000387145.1:n.1369+3001G>T | |
ENST00000413152.3:c.1276+3001G>T | ENSP00000413841.3:n.1276+3001G>T | |
NM_001080427.1:c.1276+3001G>T | NP_001073896.1:n.1276+3001G>T | |
NM_001316349.1:c.1369+3001G>T | NP_001303278.1:n.1369+3001G>T | |
NM_001316349.2:c.1369+3001G>T MANE Select | NP_001303278.1:n.1369+3001G>T |