Canonical Allele Identifier: CA1769514558
Gene:

Linked Data

dbSNP Id: rs1799796502
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734967T>C , CM000670.2:g.20734967T>C GRCh38
NC_000008.10:g.20592478T>C , CM000670.1:g.20592478T>C GRCh37
NC_000008.9:g.20636758T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949569.3:n.72-55479T>C
Search 100 bp 5'
Search 100 bp 3'