Canonical Allele Identifier: CA2756287195
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056870T>A , CM000665.2:g.53056870T>A GRCh38
NC_000003.11:g.53090886T>A , CM000665.1:g.53090886T>A GRCh37
NC_000003.10:g.53065926T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9631A>T
ENST00000607283.5:c.465-13616A>T
ENST00000607495.5:c.447+20818A>T
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