Canonical Allele Identifier: CA181547500
Gene:

Linked Data

dbSNP Id: rs986031031
MyVariant Identifiers: chr8:g.88535704G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535704G>T , CM000670.2:g.88535704G>T GRCh38
NC_000008.10:g.89547933G>T , CM000670.1:g.89547933G>T GRCh37
NC_000008.9:g.89617049G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745651.2:n.1673+10813C>A
XR_001745653.2:n.286-6976G>T
XR_928383.3:n.1475+10813C>A
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