Canonical Allele Identifier: CA14183302
Gene:

Linked Data

dbSNP Id: rs7171171
gnomAD v2: 15-38907041-A-G
gnomAD v3: 15-38614840-A-G
gnomAD v4: 15-38614840-A-G
MyVariant Identifiers: chr15:g.38907041A>G (hg19) chr15:g.38614840A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38614840A>G , CM000677.2:g.38614840A>G GRCh38
NC_000015.9:g.38907041A>G , CM000677.1:g.38907041A>G GRCh37
NC_000015.8:g.36694333A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001751736.1:n.281+2385A>G
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