HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663378C>G , CM000676.2:g.36663378C>G | GRCh38 |
NC_000014.8:g.37132583C>G , CM000676.1:g.37132583C>G | GRCh37 |
NC_000014.7:g.36202334C>G | NCBI36 |
NG_013357.1:g.10811C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000361487.7:c.486C>G MANE Select | ENSP00000355245.6:p.Tyr162Ter | |
ENST00000361487.6:c.486C>G | ENSP00000355245.6:p.Tyr162Ter | |
ENST00000402703.6:c.486C>G | ENSP00000384817.2:p.Tyr162Ter | |
ENST00000554201.1:c.-76C>G | ENSP00000450434.1:n.-76C>G | |
NM_006194.3:c.486C>G | NP_006185.1:p.Tyr162Ter | |
NM_001372076.1:c.486C>G MANE Select | NP_001359005.1:p.Tyr162Ter | |
NM_006194.4:c.486C>G | NP_006185.1:p.Tyr162Ter |