ClinGen Allele Registry
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Canonical Allele Identifier:
CA1400755767
Gene: TMED10P2
HGNC
NCBI
JSON-LD
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=
Search 100 bp 5'
Search 100 bp 3'