Canonical Allele Identifier: CA1140174081
Gene: TMCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205280322A= , CM000663.2:g.205280322A= GRCh38
NC_000001.10:g.205249450A= , CM000663.1:g.205249450A= GRCh37
NC_000001.9:g.203516073A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648708.1:n.432-27A=