ClinGen Allele Registry
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Canonical Allele Identifier:
CA890955711
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.169630994T>A
GRCh37
chr1:g.169600232T>A
Linked Data - Sequence & Population
gnomAD v3:
1:169630994 T / A
gnomAD v4:
chr1-169630994-T-A
Linked Data - NCBI & NCI
dbSNP:
3753306
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.169630994T>A , CM000663.2:g.169630994T>A
GRCh38
NC_000001.10:g.169600232T>A , CM000663.1:g.169600232T>A
GRCh37
NC_000001.9:g.167866856T>A
NCBI36
NG_012125.1:g.4146A>T
NG_012125.2:g.4146A>T
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