Canonical Allele Identifier: CA915943574
Gene:

Linked Data

ClinVar Variation Id: 660779
ClinVar RCV Id: RCV003744666
dbSNP Id: rs1580995745
gnomAD v4: 5-112707463-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707463G>T , CM000667.2:g.112707463G>T GRCh38
NC_000005.9:g.112043160G>T , CM000667.1:g.112043160G>T GRCh37
NC_000005.8:g.112071059G>T NCBI36
NG_008481.4:g.19943G>T , LRG_130:g.19943G>T
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