Canonical Allele Identifier: CA64382969
Gene:

Linked Data

dbSNP Id: rs1011039852
MyVariant Identifiers: chr2:g.200898134C>T (hg19) chr2:g.200033411C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033411C>T , CM000664.2:g.200033411C>T GRCh38
NC_000002.11:g.200898134C>T , CM000664.1:g.200898134C>T GRCh37
NC_000002.10:g.200606379C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22515G>A
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