Canonical Allele Identifier: CA2734743841
Gene:

Linked Data

dbSNP Id: rs1910120018
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477795A>G , CM000680.2:g.41477795A>G GRCh38
NC_000018.9:g.39057759A>G , CM000680.1:g.39057759A>G GRCh37
NC_000018.8:g.37311757A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935409.1:n.86-26339A>G
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