Canonical Allele Identifier: CA12186600
Gene: TRIM15 HGNC NCBI
TRIM10 HGNC NCBI

Linked Data

dbSNP Id: rs17188113
gnomAD v2: 6-30131123-T-G
gnomAD v3: 6-30163346-T-G
gnomAD v4: 6-30163346-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30163346T>G , CM000668.2:g.30163346T>G GRCh38
NC_000006.11:g.30131123T>G , CM000668.1:g.30131123T>G GRCh37
NC_000006.10:g.30239102T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376694.8:c.-339T>G (TRIM15) ENSP00000365884.4:n.-339T>G
ENST00000619857.4:c.-546T>G (TRIM15) ENSP00000484001.1:n.-546T>G
NM_033229.2:c.-339T>G (TRIM15) NP_150232.2:n.-339T>G
XM_011514224.1:c.-423+61A>C (TRIM10) XP_011512526.1:n.-423+61A>C