HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271307G= , CM000668.2:g.31271307G= | GRCh38 |
NC_000006.11:g.31239084G= , CM000668.1:g.31239084G= | GRCh37 |
NC_000006.10:g.31347063G= | NCBI36 |
NG_029422.2:g.5825C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.385C= MANE Select | ENSP00000365402.5:p.Pro129= | |
ENST00000376228.9:c.385C= | ENSP00000365402.5:p.Pro129= | |
ENST00000376237.8:c.368C= | ENSP00000365412.4:p.Ala123= | |
ENST00000383329.7:c.385C= | ENSP00000372819.3:p.Pro129= | |
ENST00000415537.1:c.383C= | ||
ENST00000484378.1:n.654C= | ||
ENST00000487245.5:n.744C= | ||
ENST00000495835.1:n.574C= | ||
NM_002117.5:c.385C= | NP_002108.4:p.Pro129= | |
NM_002117.6:c.385C= MANE Select | NP_002108.4:p.Pro129= |