Canonical Allele Identifier: CA987758024
Gene:

Linked Data

dbSNP Id: rs1969408233

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382791T>C , CM000680.2:g.10382791T>C GRCh38
NC_000018.9:g.10382788T>C , CM000680.1:g.10382788T>C GRCh37
NC_000018.8:g.10372788T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1438T>C