Canonical Allele Identifier: CA2839710366
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56262262G>T , CM000663.2:g.56262262G>T GRCh38
NC_000001.10:g.56727934G>T , CM000663.1:g.56727934G>T GRCh37
NC_000001.9:g.56500522G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.760-13062C>A ENSP00000493138.1:n.760-13062C>A
ENST00000641346.1:c.367-13062C>A
ENST00000641415.1:c.193-8369C>A
ENST00000641494.1:c.379-13062C>A
ENST00000642129.1:c.769-13062C>A
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