Canonical Allele Identifier: CA2293960176
Gene:

Linked Data

dbSNP Id: rs2031433588
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756739C>T , CM000680.2:g.31756739C>T GRCh38
NC_000018.9:g.29336702C>T , CM000680.1:g.29336702C>T GRCh37
NC_000018.8:g.27590700C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5400C>T
Search 100 bp 5'
Search 100 bp 3'