Canonical Allele Identifier: CA2000559278
Gene: TIMM8B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086729G= , CM000673.2:g.112086729G= GRCh38
NC_000011.9:g.111957453G= , CM000673.1:g.111957453G= GRCh37
NC_000011.8:g.111462663G= NCBI36
NG_012337.2:g.4883G=
NG_033145.1:g.5070C=
NG_012337.3:g.4883G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504148.3:c.-6C= MANE Select ENSP00000422122.2:n.-6C=
ENST00000504148.2:c.-6C= ENSP00000422122.2:n.-6C=
ENST00000509359.6:c.-6C= ENSP00000421964.2:n.-6C=
ENST00000541231.1:c.40C= ENSP00000438455.1:p.Arg14=
NM_012459.2:c.40C= NP_036591.2:p.Arg14=
NR_028383.1:n.70C=
NM_012459.3:c.-6C= NP_036591.3:n.-6C=
NR_028383.2:n.28C=
NR_160400.1:n.28C=
NM_012459.4:c.-6C= MANE Select NP_036591.3:n.-6C=