HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225553A>C , CM000668.2:g.3225553A>C | GRCh38 |
NC_000006.11:g.3225787A>C , CM000668.1:g.3225787A>C | GRCh37 |
NC_000006.10:g.3170786A>C | NCBI36 |
NG_016715.1:g.7182T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.536T>G MANE Select | ENSP00000259818.6:p.Val179Gly | |
ENST00000680070.1:n.1466T>G | ||
ENST00000681707.1:n.1363T>G | ||
ENST00000681757.1:n.841T>G | ||
ENST00000259818.7:c.536T>G | ENSP00000259818.6:p.Val179Gly | |
ENST00000473006.1:n.653T>G | ||
NM_178012.4:c.536T>G | NP_821080.1:p.Val179Gly | |
XM_011514571.1:c.320T>G | XP_011512873.1:p.Val107Gly | |
NM_178012.5:c.536T>G MANE Select | NP_821080.1:p.Val179Gly |