Canonical Allele Identifier: CA14152496
Gene:

Linked Data

dbSNP Id: rs17664713
gnomAD v2: 15-95318586-C-T
gnomAD v3: 15-94775357-C-T
gnomAD v4: 15-94775357-C-T
MyVariant Identifiers: chr15:g.95318586C>T (hg19) chr15:g.94775357C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94775357C>T , CM000677.2:g.94775357C>T GRCh38
NC_000015.9:g.95318586C>T , CM000677.1:g.95318586C>T GRCh37
NC_000015.8:g.93119590C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932644.1:n.369-9340G>A
XR_932644.2:n.369-9340G>A
Search 100 bp 5'
Search 100 bp 3'