Canonical Allele Identifier: CA382616357

Gene: TIMM8B

Linked Data

• MyVariant Identifiers: chr11:g.111957444C>T (hg19) ; chr11:g.112086720C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086720C>T , CM000673.2:g.112086720C>T	GRCh38
NC_000011.9:g.111957444C>T , CM000673.1:g.111957444C>T	GRCh37
NC_000011.8:g.111462654C>T	NCBI36
NG_012337.2:g.4874C>T
NG_033145.1:g.5079G>A
NG_012337.3:g.4874C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504148.3:c.4G>A MANE Select	ENSP00000422122.2:p.Ala2Thr
ENST00000504148.2:c.4G>A	ENSP00000422122.2:p.Ala2Thr
ENST00000507614.1:n.3G>A
ENST00000509359.6:c.4G>A	ENSP00000421964.2:p.Ala2Thr
ENST00000541231.1:c.49G>A	ENSP00000438455.1:p.Ala17Thr
NM_012459.2:c.49G>A	NP_036591.2:p.Ala17Thr
NR_028383.1:n.79G>A
NM_012459.3:c.4G>A	NP_036591.3:p.Ala2Thr
NR_028383.2:n.37G>A
NR_160400.1:n.37G>A
NM_012459.4:c.4G>A MANE Select	NP_036591.3:p.Ala2Thr