Canonical Allele Identifier: CA13424945
Gene: TRIM49 HGNC NCBI

Linked Data

dbSNP Id: rs2130017

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89769208C>A , CM000673.2:g.89769208C>A GRCh38
NC_000011.9:g.89502376C>A , CM000673.1:g.89502376C>A GRCh37
NC_000011.8:g.89142024C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024448617.1:c.739-372G>T XP_024304385.1:n.739-372G>T