Canonical Allele Identifier: CA275015090
Gene:

Linked Data

dbSNP Id: rs989464290
gnomAD v2: 15-87962682-G-T
gnomAD v3: 15-87419451-G-T
gnomAD v4: 15-87419451-G-T
MyVariant Identifiers: chr15:g.87962682G>T (hg19) chr15:g.87419451G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419451G>T , CM000677.2:g.87419451G>T GRCh38
NC_000015.9:g.87962682G>T , CM000677.1:g.87962682G>T GRCh37
NC_000015.8:g.85763686G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-180C>A
XR_932585.1:n.340-180C>A
XR_001751647.1:n.617-180C>A
XR_932585.2:n.627-180C>A
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