HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586506C>G , CM000673.2:g.67586506C>G | GRCh38 |
NC_000011.9:g.67353977C>G , CM000673.1:g.67353977C>G | GRCh37 |
NC_000011.8:g.67110553C>G | NCBI36 |
NG_012075.1:g.7912C>G , LRG_723:g.7912C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.454C>G | ENSP00000381604.1:p.Pro152Ala | |
ENST00000398606.10:c.562C>G MANE Select | ENSP00000381607.3:p.Pro188Ala | |
ENST00000398603.5:c.454C>G | ENSP00000381604.1:p.Pro152Ala | |
ENST00000398606.7:c.562C>G | ENSP00000381607.3:p.Pro188Ala | |
ENST00000467591.1:n.673C>G | ||
ENST00000494593.1:n.1534C>G | ||
ENST00000498765.5:c.625C>G | ||
NM_000852.3:c.562C>G , LRG_723t1:c.562C>G | NP_000843.1:p.Pro188Ala | |
NM_000852.4:c.562C>G MANE Select | NP_000843.1:p.Pro188Ala |