Canonical Allele Identifier: CA382616559

Gene: TIMM8B

Linked Data

• MyVariant Identifiers: chr11:g.111957491A>T (hg19) ; chr11:g.112086767A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086767A>T , CM000673.2:g.112086767A>T	GRCh38
NC_000011.9:g.111957491A>T , CM000673.1:g.111957491A>T	GRCh37
NC_000011.8:g.111462701A>T	NCBI36
NG_012337.2:g.4921A>T
NG_033145.1:g.5032T>A
NG_012337.3:g.4921A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504148.2:c.-44T>A	ENSP00000422122.2:n.-44T>A
ENST00000509359.6:c.-44T>A	ENSP00000421964.2:n.-44T>A
ENST00000541231.1:c.2T>A	ENSP00000438455.1:p.Met1Lys
NM_012459.2:c.2T>A	NP_036591.2:p.Met1Lys
NR_028383.1:n.32T>A