Canonical Allele Identifier: CA1769514561
Gene:

Linked Data

dbSNP Id: rs1585217564
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734970G>T , CM000670.2:g.20734970G>T GRCh38
NC_000008.10:g.20592481G>T , CM000670.1:g.20592481G>T GRCh37
NC_000008.9:g.20636761G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949569.3:n.72-55476G>T
Search 100 bp 5'
Search 100 bp 3'