HGVS | Genome Assembly |
---|---|
NC_000010.11:g.86337969A>C , CM000672.2:g.86337969A>C | GRCh38 |
NC_000010.10:g.88097726A>C , CM000672.1:g.88097726A>C | GRCh37 |
NC_000010.9:g.88087706A>C | NCBI36 |
NG_011875.1:g.33525T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327946.12:c.235+25972T>G MANE Select | ENSP00000330148.7:n.235+25972T>G | |
ENST00000327946.11:c.235+25972T>G | ENSP00000330148.7:n.235+25972T>G | |
ENST00000464741.2:c.235+25972T>G | ENSP00000433064.1:n.235+25972T>G | |
NM_017551.2:c.235+25972T>G | NP_060021.1:n.235+25972T>G | |
XM_011539720.1:c.235+25972T>G | XP_011538022.1:n.235+25972T>G | |
XM_011539720.2:c.235+25972T>G | XP_011538022.1:n.235+25972T>G | |
NM_017551.3:c.235+25972T>G MANE Select | NP_060021.1:n.235+25972T>G |