Canonical Allele Identifier: CA382616532

Gene: TIMM8B

Linked Data

• MyVariant Identifiers: chr11:g.111957485T>A (hg19) ; chr11:g.112086761T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086761T>A , CM000673.2:g.112086761T>A	GRCh38
NC_000011.9:g.111957485T>A , CM000673.1:g.111957485T>A	GRCh37
NC_000011.8:g.111462695T>A	NCBI36
NG_012337.2:g.4915T>A
NG_033145.1:g.5038A>T
NG_012337.3:g.4915T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504148.2:c.-38A>T	ENSP00000422122.2:n.-38A>T
ENST00000509359.6:c.-38A>T	ENSP00000421964.2:n.-38A>T
ENST00000541231.1:c.8A>T	ENSP00000438455.1:p.Lys3Ile
NM_012459.2:c.8A>T	NP_036591.2:p.Lys3Ile
NR_028383.1:n.38A>T