Canonical Allele Identifier: CA803406355
Gene:

Linked Data

dbSNP Id: rs1278089791
MyVariant Identifiers: chr5:g.125338417C>T (hg19) chr5:g.126002724C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002724C>T , CM000667.2:g.126002724C>T GRCh38
NC_000005.9:g.125338417C>T , CM000667.1:g.125338417C>T GRCh37
NC_000005.8:g.125366316C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3616G>A
XR_948738.1:n.497+5816G>A
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