ClinGen Allele Registry
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Canonical Allele Identifier:
CA2482512387
Gene: TMCC2
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.205280322A>T , CM000663.2:g.205280322A>T
GRCh38
NC_000001.10:g.205249450A>T , CM000663.1:g.205249450A>T
GRCh37
NC_000001.9:g.203516073A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000648708.1:n.432-27A>T
Search 100 bp 5'
Search 100 bp 3'