Canonical Allele Identifier: CA43588647
Gene:

Linked Data

dbSNP Id: rs892433057
MyVariant Identifiers: chr2:g.18025318C>T (hg19) chr2:g.17844051C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17844051C>T , CM000664.2:g.17844051C>T GRCh38
NC_000002.11:g.18025318C>T , CM000664.1:g.18025318C>T GRCh37
NC_000002.10:g.17888799C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3643G>A
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