HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177992909G>C , CM000667.2:g.177992909G>C | GRCh38 |
NC_000005.9:g.177419910G>C , CM000667.1:g.177419910G>C | GRCh37 |
NC_000005.8:g.177352516G>C | NCBI36 |
NG_015889.1:g.8334C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.481C>G MANE Select | ENSP00000311290.2:p.Pro161Ala | |
NM_006261.4:c.481C>G | NP_006252.3:p.Pro161Ala | |
NM_006261.5:c.481C>G MANE Select | NP_006252.4:p.Pro161Ala |