Canonical Allele Identifier: CA11377235
Gene: TMED10P2 HGNC NCBI

Linked Data

dbSNP Id: rs9854612

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128538371G>A , CM000665.2:g.128538371G>A GRCh38
NC_000003.11:g.128257214G>A , CM000665.1:g.128257214G>A GRCh37
NC_000003.10:g.129739904G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474255.1:n.352G>A