HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177992906G>C , CM000667.2:g.177992906G>C | GRCh38 |
NC_000005.9:g.177419907G>C , CM000667.1:g.177419907G>C | GRCh37 |
NC_000005.8:g.177352513G>C | NCBI36 |
NG_015889.1:g.8337C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000308304.2:c.484C>G MANE Select | ENSP00000311290.2:p.Pro162Ala | |
NM_006261.4:c.484C>G | NP_006252.3:p.Pro162Ala | |
NM_006261.5:c.484C>G MANE Select | NP_006252.4:p.Pro162Ala |