Canonical Allele Identifier: CA407082351
Community Standard Title: NM_001985.3(ETFB):c.375+1G>T
Gene: ETFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51353131C>A , CM000681.2:g.51353131C>A GRCh38
NC_000019.9:g.51856385C>A , CM000681.1:g.51856385C>A GRCh37
NC_000019.8:g.56548197C>A NCBI36
NG_007115.1:g.18288G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001985.3:c.375+1G>T MANE Select NP_001976.1:n.375+1G>T
ENST00000309244.9:c.375+1G>T MANE Select ENSP00000311930.3:n.375+1G>T
NM_001014763.1:c.648+1G>T NP_001014763.1:n.648+1G>T
NM_001985.2:c.375+1G>T NP_001976.1:n.375+1G>T
ENST00000309244.8:c.375+1G>T ENSP00000311930.3:n.375+1G>T
ENST00000354232.8:c.648+1G>T ENSP00000346173.3:n.648+1G>T
ENST00000593992.1:n.398+1G>T
ENST00000596253.1:c.216+1019G>T ENSP00000469628.1:n.216+1019G>T
ENST00000600067.1:c.*301+1G>T ENSP00000469452.1:n.*301+1G>T
XM_024451418.1:c.264+1G>T XP_024307186.1:n.264+1G>T