Canonical Allele Identifier: CA427349511
Gene:

Linked Data

dbSNP Id: rs759968607
gnomAD v3: 2-88016427-C-A
gnomAD v4: 2-88016427-C-A
MyVariant Identifiers: chr2:g.88315946C>A (hg19) chr2:g.88016427C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016427C>A , CM000664.2:g.88016427C>A GRCh38
NC_000002.11:g.88315946C>A , CM000664.1:g.88315946C>A GRCh37
NC_000002.10:g.88097061C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.772C>A
XR_940336.3:n.772C>A
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