Canonical Allele Identifier: CA2580596893
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12108916G>T , CM000671.2:g.12108916G>T GRCh38
NC_000009.11:g.12108916G>T , CM000671.1:g.12108916G>T GRCh37
NC_000009.10:g.12098916G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929481.1:n.166+7905C>A
XR_929482.1:n.260+7905C>A
XR_929481.2:n.166+7905C>A
XR_929482.2:n.260+7905C>A
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