HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271377C>G , CM000668.2:g.31271377C>G | GRCh38 |
NC_000006.11:g.31239154C>G , CM000668.1:g.31239154C>G | GRCh37 |
NC_000006.10:g.31347133C>G | NCBI36 |
NG_029422.2:g.5755G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.344-29G>C MANE Select | ENSP00000365402.5:n.344-29G>C | |
ENST00000376228.9:c.344-29G>C | ENSP00000365402.5:n.344-29G>C | |
ENST00000376237.8:c.344-46G>C | ENSP00000365412.4:n.344-46G>C | |
ENST00000383329.7:c.344-29G>C | ENSP00000372819.3:n.344-29G>C | |
ENST00000415537.1:c.342-29G>C | ||
ENST00000484378.1:n.584G>C | ||
ENST00000487245.5:n.674G>C | ||
ENST00000495835.1:n.533-29G>C | ||
NM_002117.5:c.344-29G>C | NP_002108.4:n.344-29G>C | |
NM_002117.6:c.344-29G>C MANE Select | NP_002108.4:n.344-29G>C |