Canonical Allele Identifier: CA894253987
Gene:

Linked Data

dbSNP Id: rs1397692818
MyVariant Identifiers: chr2:g.88315477A>T (hg19) chr2:g.88015958A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015958A>T , CM000664.2:g.88015958A>T GRCh38
NC_000002.11:g.88315477A>T , CM000664.1:g.88315477A>T GRCh37
NC_000002.10:g.88096592A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.303A>T
XR_940336.3:n.303A>T
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Search 100 bp 3'