Canonical Allele Identifier: CA1365145742
Gene:

Linked Data

dbSNP Id: rs1700429982
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057276G>A , CM000665.2:g.53057276G>A GRCh38
NC_000003.11:g.53091292G>A , CM000665.1:g.53091292G>A GRCh37
NC_000003.10:g.53066332G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-10037C>T
ENST00000607283.5:c.465-14022C>T
ENST00000607495.5:c.447+20412C>T
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