Canonical Allele Identifier: CA275015098
Gene:

Linked Data

dbSNP Id: rs940947451
MyVariant Identifiers: chr15:g.87962732C>T (hg19) chr15:g.87419501C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419501C>T , CM000677.2:g.87419501C>T GRCh38
NC_000015.9:g.87962732C>T , CM000677.1:g.87962732C>T GRCh37
NC_000015.8:g.85763736C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.339+228G>A
XR_932585.1:n.339+228G>A
XR_001751647.1:n.616+228G>A
XR_932585.2:n.626+228G>A
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