Canonical Allele Identifier: CA528893602
Gene:

Linked Data

dbSNP Id: rs1352979233
gnomAD v2: 1-213855609-A-G
gnomAD v3: 1-213682266-A-G
gnomAD v4: 1-213682266-A-G
MyVariant Identifiers: chr1:g.213855609A>G (hg19) chr1:g.213682266A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682266A>G , CM000663.2:g.213682266A>G GRCh38
NC_000001.10:g.213855609A>G , CM000663.1:g.213855609A>G GRCh37
NC_000001.9:g.211922232A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49151A>G
XR_001738464.1:n.426-49151A>G
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