Canonical Allele Identifier: CA1400755767
Gene: TMED10P2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000474255.1:n.352G=