Canonical Allele Identifier: CA1350284132
Gene:

Linked Data

dbSNP Id: rs1230696279
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207232C>T , CM000665.2:g.21207232C>T GRCh38
NC_000003.11:g.21248724C>T , CM000665.1:g.21248724C>T GRCh37
NC_000003.10:g.21223728C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940646.1:n.254-3766C>T
XR_940646.2:n.547-3766C>T
Search 100 bp 5'
Search 100 bp 3'