Canonical Allele Identifier: CA2000559262

Gene: TIMM8B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086725G= , CM000673.2:g.112086725G=	GRCh38
NC_000011.9:g.111957449G= , CM000673.1:g.111957449G=	GRCh37
NC_000011.8:g.111462659G=	NCBI36
NG_012337.2:g.4879G=
NG_033145.1:g.5074C=
NG_012337.3:g.4879G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504148.3:c.-2C= MANE Select	ENSP00000422122.2:n.-2C=
ENST00000504148.2:c.-2C=	ENSP00000422122.2:n.-2C=
ENST00000509359.6:c.-2C=	ENSP00000421964.2:n.-2C=
ENST00000541231.1:c.44C=	ENSP00000438455.1:p.Thr15=
NM_012459.2:c.44C=	NP_036591.2:p.Thr15=
NR_028383.1:n.74C=
NM_012459.3:c.-2C=	NP_036591.3:n.-2C=
NR_028383.2:n.32C=
NR_160400.1:n.32C=
NM_012459.4:c.-2C= MANE Select	NP_036591.3:n.-2C=