HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2315456C= , CM000678.2:g.2315456C= | GRCh38 |
NC_000016.9:g.2365457C= , CM000678.1:g.2365457C= | GRCh37 |
NC_000016.8:g.2305458C= | NCBI36 |
NG_011790.1:g.30291G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301732.10:c.1111+1827G= MANE Select | ENSP00000301732.5:n.1111+1827G= | |
ENST00000301732.9:c.1111+1827G= | ENSP00000301732.5:n.1111+1827G= | |
ENST00000382381.7:c.1111+1827G= | ENSP00000371818.3:n.1111+1827G= | |
ENST00000563623.5:n.1674+1827G= | ||
NM_001089.2:c.1111+1827G= | NP_001080.2:n.1111+1827G= | |
NM_001089.3:c.1111+1827G= MANE Select | NP_001080.2:n.1111+1827G= |