Canonical Allele Identifier: CA476788969

Gene: TIMM8B

Linked Data

• MyVariant Identifiers: chr11:g.111957448T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086724T>A , CM000673.2:g.112086724T>A	GRCh38
NC_000011.9:g.111957448T>A , CM000673.1:g.111957448T>A	GRCh37
NC_000011.8:g.111462658T>A	NCBI36
NG_012337.2:g.4878T>A
NG_033145.1:g.5075A>T
NG_012337.3:g.4878T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504148.3:c.-1A>T MANE Select	ENSP00000422122.2:n.-1A>T
ENST00000504148.2:c.-1A>T	ENSP00000422122.2:n.-1A>T
ENST00000509359.6:c.-1A>T	ENSP00000421964.2:n.-1A>T
ENST00000541231.1:c.45A>T	ENSP00000438455.1:p.Thr15=
NM_012459.2:c.45A>T	NP_036591.2:p.Thr15=
NR_028383.1:n.75A>T
NM_012459.3:c.-1A>T	NP_036591.3:n.-1A>T
NR_028383.2:n.33A>T
NR_160400.1:n.33A>T
NM_012459.4:c.-1A>T MANE Select	NP_036591.3:n.-1A>T