Canonical Allele Identifier: CA1649534285
Gene:

Linked Data

dbSNP Id: rs1457500385
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102523G>A , CM000668.2:g.98102523G>A GRCh38
NC_000006.11:g.98550399G>A , CM000668.1:g.98550399G>A GRCh37
NC_000006.10:g.98657120G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3253G>A
XR_942809.1:n.456+3253G>A
Search 100 bp 5'
Search 100 bp 3'