Canonical Allele Identifier: CA43254741
Gene:

Linked Data

dbSNP Id: rs866914043
MyVariant Identifiers: chr2:g.16639543T>G (hg19) chr2:g.16458275T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458275T>G , CM000664.2:g.16458275T>G GRCh38
NC_000002.11:g.16639543T>G , CM000664.1:g.16639543T>G GRCh37
NC_000002.10:g.16503024T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3181A>C
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