Canonical Allele Identifier: CA2284239340
Gene:

Linked Data

dbSNP Id: rs1598367283

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321242T>C , CM000680.2:g.10321242T>C GRCh38
NC_000018.9:g.10321239T>C , CM000680.1:g.10321239T>C GRCh37
NC_000018.8:g.10311239T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+906A>G
XR_001753344.1:n.650+906A>G
XR_001753345.1:n.879A>G
XR_001753346.1:n.549+906A>G