HGVS | Genome Assembly |
---|---|
NC_000020.11:g.6778376G>C , CM000682.2:g.6778376G>C | GRCh38 |
NC_000020.10:g.6759023G>C , CM000682.1:g.6759023G>C | GRCh37 |
NC_000020.9:g.6707023G>C | NCBI36 |
NG_023233.1:g.15279G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378827.5:c.478G>C MANE Select | ENSP00000368104.3:p.Ala160Pro | |
ENST00000378827.4:c.478G>C | ENSP00000368104.3:p.Ala160Pro | |
NM_001200.2:c.478G>C | NP_001191.1:p.Ala160Pro | |
XM_011529323.1:c.10G>C | XP_011527625.1:p.Ala4Pro | |
NM_001200.3:c.478G>C | NP_001191.1:p.Ala160Pro | |
NM_001200.4:c.478G>C MANE Select | NP_001191.1:p.Ala160Pro |