Canonical Allele Identifier: CA15077767
Gene:

Linked Data

ClinVar Variation Id: 440703
ClinVar RCV Id: RCV000508949
dbSNP Id: rs2479409
gnomAD v2: 1-55504650-G-A
gnomAD v3: 1-55038977-G-A
gnomAD v4: 1-55038977-G-A
MyVariant Identifiers: chr1:g.55504650G>A (hg19) chr1:g.55038977G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55038977G>A , CM000663.2:g.55038977G>A GRCh38
NC_000001.10:g.55504650G>A , CM000663.1:g.55504650G>A GRCh37
NC_000001.9:g.55277238G>A NCBI36
NG_009061.1:g.4431G>A , LRG_275:g.4431G>A
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