HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31270400C>G , CM000668.2:g.31270400C>G | GRCh38 |
NC_000006.11:g.31238177C>G , CM000668.1:g.31238177C>G | GRCh37 |
NC_000006.10:g.31346156C>G | NCBI36 |
NG_029422.2:g.6732G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.705G>C MANE Select | ENSP00000365402.5:p.Ala235= | |
ENST00000376228.9:c.705G>C | ENSP00000365402.5:p.Ala235= | |
ENST00000376237.8:c.*292G>C | ENSP00000365412.4:n.*292G>C | |
ENST00000383329.7:c.705G>C | ENSP00000372819.3:p.Ala235= | |
ENST00000415537.1:c.664+39G>C | ||
ENST00000470363.5:n.23G>C | ||
ENST00000487245.5:n.1064G>C | ||
ENST00000495835.1:n.894G>C | ||
NM_002117.5:c.705G>C | NP_002108.4:p.Ala235= | |
NM_002117.6:c.705G>C MANE Select | NP_002108.4:p.Ala235= |