Canonical Allele Identifier: CA2000559280
Gene: TIMM8B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086730C= , CM000673.2:g.112086730C= GRCh38
NC_000011.9:g.111957454C= , CM000673.1:g.111957454C= GRCh37
NC_000011.8:g.111462664C= NCBI36
NG_012337.2:g.4884C=
NG_033145.1:g.5069G=
NG_012337.3:g.4884C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504148.3:c.-7G= MANE Select ENSP00000422122.2:n.-7G=
ENST00000504148.2:c.-7G= ENSP00000422122.2:n.-7G=
ENST00000509359.6:c.-7G= ENSP00000421964.2:n.-7G=
ENST00000541231.1:c.39G= ENSP00000438455.1:p.Arg13=
NM_012459.2:c.39G= NP_036591.2:p.Arg13=
NR_028383.1:n.69G=
NM_012459.3:c.-7G= NP_036591.3:n.-7G=
NR_028383.2:n.27G=
NR_160400.1:n.27G=
NM_012459.4:c.-7G= MANE Select NP_036591.3:n.-7G=