HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32475114T= , CM000684.2:g.32475114T= | GRCh38 |
NC_000022.10:g.32871101T= , CM000684.1:g.32871101T= | GRCh37 |
NC_000022.9:g.31201101T= | NCBI36 |
NG_016001.1:g.5395T= | |
NG_016001.2:g.5395T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266087.12:c.112T= MANE Select | ENSP00000266087.7:p.Trp38= | |
ENST00000266087.11:c.112T= | ENSP00000266087.7:p.Trp38= | |
ENST00000420700.5:c.112T= | ENSP00000406155.1:p.Trp38= | |
ENST00000425028.5:c.112T= | ENSP00000395823.1:p.Trp38= | |
ENST00000492535.1:n.100T= | ||
NM_012179.3:c.112T= | NP_036311.3:p.Trp38= | |
XM_011530106.1:c.-62T= | XP_011528408.1:n.-62T= | |
XM_024452207.1:c.-79T= | XP_024307975.1:n.-79T= | |
NM_012179.4:c.112T= MANE Select | NP_036311.3:p.Trp38= |