HGVS | Genome Assembly |
---|---|
NC_000004.12:g.121696978A>C , CM000666.2:g.121696978A>C | GRCh38 |
NC_000004.11:g.122618133A>C , CM000666.1:g.122618133A>C | GRCh37 |
NC_000004.10:g.122837583A>C | NCBI36 |
NG_032042.1:g.5015T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000296511.10:c.-151T>G MANE Select | ENSP00000296511.5:n.-151T>G | |
ENST00000296511.9:c.-151T>G | ENSP00000296511.5:n.-151T>G | |
ENST00000509016.5:n.15T>G | ||
ENST00000513428.5:n.15T>G | ||
ENST00000513523.1:n.18T>G | ||
NM_001154.3:c.-151T>G | NP_001145.1:n.-151T>G | |
XM_017008141.2:c.-151T>G | XP_016863630.1:n.-151T>G | |
NM_001154.4:c.-151T>G MANE Select | NP_001145.1:n.-151T>G |