Canonical Allele Identifier: CA2606896455
Gene:

Linked Data

dbSNP Id: rs2108529002

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931486A>G , CM000665.2:g.187931486A>G GRCh38
NC_000003.11:g.187649274A>G , CM000665.1:g.187649274A>G GRCh37
NC_000003.10:g.189131968A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1428T>C