Canonical Allele Identifier: CA382616366

Gene: TIMM8B

Linked Data

• MyVariant Identifiers: chr11:g.111957446A>C (hg19) ; chr11:g.112086722A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086722A>C , CM000673.2:g.112086722A>C	GRCh38
NC_000011.9:g.111957446A>C , CM000673.1:g.111957446A>C	GRCh37
NC_000011.8:g.111462656A>C	NCBI36
NG_012337.2:g.4876A>C
NG_033145.1:g.5077T>G
NG_012337.3:g.4876A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504148.3:c.2T>G MANE Select	ENSP00000422122.2:p.Met1Arg
ENST00000504148.2:c.2T>G	ENSP00000422122.2:p.Met1Arg
ENST00000507614.1:n.1T>G
ENST00000509359.6:c.2T>G	ENSP00000421964.2:p.Met1Arg
ENST00000541231.1:c.47T>G	ENSP00000438455.1:p.Met16Arg
NM_012459.2:c.47T>G	NP_036591.2:p.Met16Arg
NR_028383.1:n.77T>G
NM_012459.3:c.2T>G	NP_036591.3:p.Met1Arg
NR_028383.2:n.35T>G
NR_160400.1:n.35T>G
NM_012459.4:c.2T>G MANE Select	NP_036591.3:p.Met1Arg