HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47332637G>T , CM000673.2:g.47332637G>T | GRCh38 |
NC_000011.9:g.47354188G>T , CM000673.1:g.47354188G>T | GRCh37 |
NC_000011.8:g.47310764G>T | NCBI36 |
NG_007667.1:g.25066C>A , LRG_386:g.25066C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.3556C>A MANE Select | ENSP00000442795.1:p.Pro1186Thr | |
ENST00000256993.8:c.3556C>A | ENSP00000256993.5:p.Pro1186Thr | |
ENST00000399249.6:c.3556C>A | ENSP00000382193.2:p.Pro1186Thr | |
ENST00000545968.5:c.3556C>A | ENSP00000442795.1:p.Pro1186Thr | |
NM_000256.3:c.3556C>A , LRG_386t1:c.3556C>A MANE Select | NP_000247.2:p.Pro1186Thr | |
XM_011520117.1:c.3538C>A | XP_011518419.1:p.Pro1180Thr | |
XM_011520118.1:c.3475C>A | XP_011518420.1:p.Pro1159Thr |