Canonical Allele Identifier: CA1573933695
Gene:

Linked Data

dbSNP Id: rs1780063285
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661011C>G , CM000667.2:g.113661011C>G GRCh38
NC_000005.9:g.112996708C>G , CM000667.1:g.112996708C>G GRCh37
NC_000005.8:g.113024607C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27647C>G
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