Canonical Allele Identifier: CA2293960132
Gene:

Linked Data

dbSNP Id: rs2031432583

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756629T>C , CM000680.2:g.31756629T>C GRCh38
NC_000018.9:g.29336592T>C , CM000680.1:g.29336592T>C GRCh37
NC_000018.8:g.27590590T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5510T>C