Canonical Allele Identifier: CA806430632
Gene:

Linked Data

dbSNP Id: rs1160128752
MyVariant Identifiers: chr5:g.159008019C>A (hg19) chr5:g.159581012C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159581012C>A , CM000667.2:g.159581012C>A GRCh38
NC_000005.9:g.159008019C>A , CM000667.1:g.159008019C>A GRCh37
NC_000005.8:g.158940597C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+577C>A
XR_941140.1:n.2075+577C>A
XR_941141.1:n.570+577C>A
XR_941139.2:n.2229+577C>A
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