Canonical Allele Identifier: CA9610811
Community Standard Title: NM_001985.3(ETFB):c.253C>T (p.Arg85Ter)
Gene: ETFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51353254G>A , CM000681.2:g.51353254G>A GRCh38
NC_000019.9:g.51856508G>A , CM000681.1:g.51856508G>A GRCh37
NC_000019.8:g.56548320G>A NCBI36
NG_007115.1:g.18165C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001985.3:c.253C>T MANE Select NP_001976.1:p.Arg85Ter
ENST00000309244.9:c.253C>T MANE Select ENSP00000311930.3:p.Arg85Ter
NM_001014763.1:c.526C>T NP_001014763.1:p.Arg176Ter
NM_001985.2:c.253C>T NP_001976.1:p.Arg85Ter
ENST00000309244.8:c.253C>T ENSP00000311930.3:p.Arg85Ter
ENST00000354232.8:c.526C>T ENSP00000346173.3:p.Arg176Ter
ENST00000593992.1:n.276C>T
ENST00000596253.1:c.216+896C>T ENSP00000469628.1:n.216+896C>T
ENST00000600067.1:c.*179C>T ENSP00000469452.1:n.*179C>T
XM_024451418.1:c.142C>T XP_024307186.1:p.Arg48Ter