Canonical Allele Identifier: CA1190159227

Gene: TRIM33

Linked Data

• dbSNP Id: rs1651494756

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114395482A>G , CM000663.2:g.114395482A>G	GRCh38
NC_000001.10:g.114938104A>G , CM000663.1:g.114938104A>G	GRCh37
NC_000001.9:g.114739627A>G	NCBI36
NG_023287.1:g.120678T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000358465.7:c.*2166T>C MANE Select	ENSP00000351250.2:n.*2166T>C
ENST00000358465.6:c.*2166T>C	ENSP00000351250.2:n.*2166T>C
NM_015906.3:c.*2166T>C	NP_056990.3:n.*2166T>C
NM_033020.2:c.*2166T>C	NP_148980.2:n.*2166T>C
XM_005270936.2:c.*2166T>C	XP_005270993.1:n.*2166T>C
XM_005270937.2:c.*2166T>C	XP_005270994.1:n.*2166T>C
XM_011541568.1:c.*2166T>C	XP_011539870.1:n.*2166T>C
XM_005270936.4:c.*2166T>C	XP_005270993.1:n.*2166T>C
XM_005270937.4:c.*2166T>C	XP_005270994.1:n.*2166T>C
XM_011541568.3:c.*2166T>C	XP_011539870.1:n.*2166T>C
NM_015906.4:c.*2166T>C MANE Select	NP_056990.3:n.*2166T>C
NM_033020.3:c.*2166T>C	NP_148980.2:n.*2166T>C