Canonical Allele Identifier: CA51878267
Gene:

Linked Data

dbSNP Id: rs1002277676
MyVariant Identifiers: chr2:g.88016090G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016090G>A , CM000664.2:g.88016090G>A GRCh38
NC_000002.11:g.88315609G>A , CM000664.1:g.88315609G>A GRCh37
NC_000002.10:g.88096724G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.435G>A
XR_940336.3:n.435G>A
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Search 100 bp 3'