Canonical Allele Identifier: CA716729388
Gene:

Linked Data

dbSNP Id: rs1237528255
MyVariant Identifiers: chr15:g.87962731T>G (hg19) chr15:g.87419500T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419500T>G , CM000677.2:g.87419500T>G GRCh38
NC_000015.9:g.87962731T>G , CM000677.1:g.87962731T>G GRCh37
NC_000015.8:g.85763735T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-229A>C
XR_932585.1:n.340-229A>C
XR_001751647.1:n.617-229A>C
XR_932585.2:n.627-229A>C
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