HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6145560T>C , CM000668.2:g.6145560T>C | GRCh38 |
NC_000006.11:g.6145793T>C , CM000668.1:g.6145793T>C | GRCh37 |
NC_000006.10:g.6090792T>C | NCBI36 |
NG_008107.1:g.180132A>G , LRG_549:g.180132A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264870.8:c.*59A>G MANE Select | ENSP00000264870.3:n.*59A>G | |
ENST00000264870.7:c.*59A>G | ENSP00000264870.3:n.*59A>G | |
NM_000129.3:c.*59A>G , LRG_549t1:c.*59A>G | NP_000120.2:n.*59A>G | |
XM_006715010.2:c.*59A>G | XP_006715073.1:n.*59A>G | |
XM_011514342.1:c.*59A>G | XP_011512644.1:n.*59A>G | |
NM_000129.4:c.*59A>G MANE Select | NP_000120.2:n.*59A>G |