Canonical Allele Identifier: CA1190159221
Gene: TRIM33 HGNC NCBI

Linked Data

dbSNP Id: rs1651494134
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114395476A>T , CM000663.2:g.114395476A>T GRCh38
NC_000001.10:g.114938098A>T , CM000663.1:g.114938098A>T GRCh37
NC_000001.9:g.114739621A>T NCBI36
NG_023287.1:g.120684T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358465.7:c.*2172T>A MANE Select ENSP00000351250.2:n.*2172T>A
ENST00000358465.6:c.*2172T>A ENSP00000351250.2:n.*2172T>A
NM_015906.3:c.*2172T>A NP_056990.3:n.*2172T>A
NM_033020.2:c.*2172T>A NP_148980.2:n.*2172T>A
XM_005270936.2:c.*2172T>A XP_005270993.1:n.*2172T>A
XM_005270937.2:c.*2172T>A XP_005270994.1:n.*2172T>A
XM_011541568.1:c.*2172T>A XP_011539870.1:n.*2172T>A
XM_005270936.4:c.*2172T>A XP_005270993.1:n.*2172T>A
XM_005270937.4:c.*2172T>A XP_005270994.1:n.*2172T>A
XM_011541568.3:c.*2172T>A XP_011539870.1:n.*2172T>A
NM_015906.4:c.*2172T>A MANE Select NP_056990.3:n.*2172T>A
NM_033020.3:c.*2172T>A NP_148980.2:n.*2172T>A
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