Canonical Allele Identifier: CA64382886
Gene:

Linked Data

dbSNP Id: rs899384611
gnomAD v3: 2-200033165-C-T
gnomAD v4: 2-200033165-C-T
MyVariant Identifiers: chr2:g.200897888C>T (hg19) chr2:g.200033165C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033165C>T , CM000664.2:g.200033165C>T GRCh38
NC_000002.11:g.200897888C>T , CM000664.1:g.200897888C>T GRCh37
NC_000002.10:g.200606133C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22269G>A
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