Canonical Allele Identifier: CA296576134
Gene:

Linked Data

dbSNP Id: rs900120554
MyVariant Identifiers: chr18:g.10382791T>A (hg19) chr18:g.10382794T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382794T>A , CM000680.2:g.10382794T>A GRCh38
NC_000018.9:g.10382791T>A , CM000680.1:g.10382791T>A GRCh37
NC_000018.8:g.10372791T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1441T>A
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