HGVS | Genome Assembly |
---|---|
NC_000017.11:g.27797739G>A , CM000679.2:g.27797739G>A | GRCh38 |
NC_000017.10:g.26124765G>A , CM000679.1:g.26124765G>A | GRCh37 |
NC_000017.9:g.23148892G>A | NCBI36 |
NG_011470.1:g.7791C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000697337.1:c.110+961C>T | ENSP00000513259.1:n.110+961C>T | |
ENST00000313735.11:c.110+961C>T MANE Select | ENSP00000327251.6:n.110+961C>T | |
ENST00000313735.10:c.110+961C>T | ENSP00000327251.6:n.110+961C>T | |
ENST00000621962.1:c.110+961C>T | ENSP00000482291.1:n.110+961C>T | |
NM_000625.4:c.110+961C>T MANE Select | NP_000616.3:n.110+961C>T | |
XM_011524859.1:c.110+961C>T | XP_011523161.1:n.110+961C>T | |
XM_011524861.1:c.110+961C>T | XP_011523163.1:n.110+961C>T |