Canonical Allele Identifier: CA2733853825
Gene:

Linked Data

dbSNP Id: rs2144842542
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788878C>T , CM000679.2:g.57788878C>T GRCh38
NC_000017.10:g.55866239C>T , CM000679.1:g.55866239C>T GRCh37
NC_000017.9:g.53221238C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934881.1:n.1608-16682G>A
XR_934881.3:n.3815-16682G>A
Search 100 bp 5'
Search 100 bp 3'