Canonical Allele Identifier: CA806430630
Gene:

Linked Data

dbSNP Id: rs1324125310
MyVariant Identifiers: chr5:g.159008004C>G (hg19) chr5:g.159580997C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580997C>G , CM000667.2:g.159580997C>G GRCh38
NC_000005.9:g.159008004C>G , CM000667.1:g.159008004C>G GRCh37
NC_000005.8:g.158940582C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+562C>G
XR_941140.1:n.2075+562C>G
XR_941141.1:n.570+562C>G
XR_941139.2:n.2229+562C>G
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