ClinGen Allele Registry
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Canonical Allele Identifier:
CA1842217827
Gene: CTAGE12P
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.27610659A= , CM000671.2:g.27610659A=
GRCh38
NC_000009.11:g.27610657A= , CM000671.1:g.27610657A=
GRCh37
NC_000009.10:g.27600657A=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000400348.3:n.87T=
Search 100 bp 5'
Search 100 bp 3'