HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32475105C>T , CM000684.2:g.32475105C>T | GRCh38 |
NC_000022.10:g.32871092C>T , CM000684.1:g.32871092C>T | GRCh37 |
NC_000022.9:g.31201092C>T | NCBI36 |
NG_016001.1:g.5386C>T | |
NG_016001.2:g.5386C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266087.12:c.103C>T MANE Select | ENSP00000266087.7:p.Leu35= | |
ENST00000266087.11:c.103C>T | ENSP00000266087.7:p.Leu35= | |
ENST00000420700.5:c.103C>T | ENSP00000406155.1:p.Leu35= | |
ENST00000425028.5:c.103C>T | ENSP00000395823.1:p.Leu35= | |
ENST00000492535.1:n.91C>T | ||
NM_012179.3:c.103C>T | NP_036311.3:p.Leu35= | |
XM_011530106.1:c.-71C>T | XP_011528408.1:n.-71C>T | |
XM_024452207.1:c.-88C>T | XP_024307975.1:n.-88C>T | |
NM_012179.4:c.103C>T MANE Select | NP_036311.3:p.Leu35= |