ClinGen Allele Registry
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Canonical Allele Identifier:
CA786414646
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122589881_122589883del
GRCh37
chr4:g.123511036_123511038del
Linked Data - NCBI & NCI
dbSNP:
1355633179
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122589881_122589883del , CM000666.2:g.122589881_122589883del
GRCh38
NC_000004.11:g.123511036_123511038del , CM000666.1:g.123511036_123511038del
GRCh37
NC_000004.10:g.123730486_123730488del
NCBI36
Search 100 bp 5'
Search 100 bp 3'