ClinGen Allele Registry
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Canonical Allele Identifier:
CA706895451
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.54390568G>T
GRCh37
chr14:g.54857286G>T
Linked Data - NCBI & NCI
dbSNP:
4293296
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.54390568G>T , CM000676.2:g.54390568G>T
GRCh38
NC_000014.8:g.54857286G>T , CM000676.1:g.54857286G>T
GRCh37
NC_000014.7:g.53927036G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'