Canonical Allele Identifier: CA2293960105
Gene:

Linked Data

dbSNP Id: rs2031431747

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756554A>C , CM000680.2:g.31756554A>C GRCh38
NC_000018.9:g.29336517A>C , CM000680.1:g.29336517A>C GRCh37
NC_000018.8:g.27590515A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5585A>C