Canonical Allele Identifier: CA2580913176
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.7047054A>T , CM000672.2:g.7047054A>T GRCh38
NC_000010.10:g.7089016A>T , CM000672.1:g.7089016A>T GRCh37
NC_000010.9:g.7129022A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930623.1:n.173-16737T>A
XR_930624.1:n.171-16737T>A
XR_930625.1:n.172-16737T>A
XR_930626.1:n.168-16737T>A
XR_930627.1:n.173-16737T>A
XR_001747351.1:n.364-16737T>A
XR_001747352.1:n.364-16737T>A
XR_001747353.1:n.188-34398T>A
XR_001747354.1:n.364-16737T>A
XR_930623.2:n.364-16737T>A
XR_930624.2:n.364-16737T>A
XR_930625.2:n.364-16737T>A
XR_930626.2:n.364-16737T>A
XR_930627.2:n.364-16737T>A
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