HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2315432A>C , CM000678.2:g.2315432A>C | GRCh38 |
NC_000016.9:g.2365433A>C , CM000678.1:g.2365433A>C | GRCh37 |
NC_000016.8:g.2305434A>C | NCBI36 |
NG_011790.1:g.30315T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301732.10:c.1111+1851T>G MANE Select | ENSP00000301732.5:n.1111+1851T>G | |
ENST00000301732.9:c.1111+1851T>G | ENSP00000301732.5:n.1111+1851T>G | |
ENST00000382381.7:c.1111+1851T>G | ENSP00000371818.3:n.1111+1851T>G | |
ENST00000563623.5:n.1674+1851T>G | ||
NM_001089.2:c.1111+1851T>G | NP_001080.2:n.1111+1851T>G | |
NM_001089.3:c.1111+1851T>G MANE Select | NP_001080.2:n.1111+1851T>G |