Canonical Allele Identifier: CA3099345721
Gene: TMEM212 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.171936113C= , CM000665.2:g.171936113C= GRCh38
NC_000003.11:g.171653903C= , CM000665.1:g.171653903C= GRCh37
NC_000003.10:g.173136597C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420375.5:c.702-1925C=
ENST00000469981.1:n.409-1925C=
XR_924719.1:n.409-1925C=
XR_924719.2:n.456-1925C=