ClinGen Allele Registry
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Canonical Allele Identifier:
CA2189889591
Gene: ANKRD34C-AS1
HGNC
NCBI
Linked Data - NCBI & NCI
dbSNP:
4779031
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.79241030C>T , CM000677.2:g.79241030C>T
GRCh38
NC_000015.9:g.79533372C>T , CM000677.1:g.79533372C>T
GRCh37
NC_000015.8:g.77320427C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038997.1:n.297+42619G>A
Search 100 bp 5'
Search 100 bp 3'