Canonical Allele Identifier: CA2284269265
Gene:

Linked Data

dbSNP Id: rs1940763725

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382786A>C , CM000680.2:g.10382786A>C GRCh38
NC_000018.9:g.10382783A>C , CM000680.1:g.10382783A>C GRCh37
NC_000018.8:g.10372783A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1433A>C