Canonical Allele Identifier: CA2702864578
Gene:

Linked Data

dbSNP Id: rs1157652402

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266854A>G , CM000665.2:g.72266854A>G GRCh38
NC_000003.11:g.72316005A>G , CM000665.1:g.72316005A>G GRCh37
NC_000003.10:g.72398695A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8254T>C