Canonical Allele Identifier: CA106421578
Gene:

Linked Data

dbSNP Id: rs559588901
MyVariant Identifiers: chr4:g.135522594C>G (hg19) chr4:g.134601439C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601439C>G , CM000666.2:g.134601439C>G GRCh38
NC_000004.11:g.135522594C>G , CM000666.1:g.135522594C>G GRCh37
NC_000004.10:g.135742044C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14080C>G
XR_939214.1:n.392+14080C>G
XR_939214.2:n.392+14080C>G
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