Canonical Allele Identifier: CA2004281823
Gene: TRIM29 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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