Canonical Allele Identifier: CA222002620
Gene:

Linked Data

dbSNP Id: rs1015934690
MyVariant Identifiers: chr11:g.45528089C>T (hg19) chr11:g.45506539C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506539C>T , CM000673.2:g.45506539C>T GRCh38
NC_000011.9:g.45528089C>T , CM000673.1:g.45528089C>T GRCh37
NC_000011.8:g.45484665C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16768G>A
XR_931245.3:n.566-16768G>A
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