Canonical Allele Identifier: CA2004281822
Community Standard Title: NC_000011.10:g.120156040G=
Gene: TRIM29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.120156040G= , CM000673.2:g.120156040G= GRCh38
NC_000011.9:g.120026748G= , CM000673.1:g.120026748G= GRCh37
NC_000011.8:g.119531958G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000529040.1:c.-114-17895C= ENSP00000433084.1:n.-114-17895C=
ENST00000532833.1:c.-114-17895C= ENSP00000436567.1:n.-114-17895C=
XM_011542731.1:c.-114-17895C= XP_011541033.1:n.-114-17895C=