ClinGen Allele Registry
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Canonical Allele Identifier:
CA14662613
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.44905307A>T
GRCh37
chr19:g.45408564A>T
Linked Data - Sequence & Population
gnomAD v2:
19:45408564 A / T
gnomAD v3:
19:44905307 A / T
gnomAD v4:
chr19-44905307-A-T
Joint Max Group AF
0.31120101 (MID)
Genomes Max Group AF
0.29315392 (AFR)
Linked Data - NCBI & NCI
dbSNP:
449647
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.44905307A>T , CM000681.2:g.44905307A>T
GRCh38
NC_000019.9:g.45408564A>T , CM000681.1:g.45408564A>T
GRCh37
NC_000019.8:g.50100404A>T
NCBI36
NG_007084.2:g.4526A>T
NG_042854.1:g.19088A>T
Search 100 bp 5'
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