Canonical Allele Identifier: CA2355978809
Gene:

Linked Data

dbSNP Id: rs1600374638

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661869T>G , CM000682.2:g.23661869T>G GRCh38
NC_000020.10:g.23642506T>G , CM000682.1:g.23642506T>G GRCh37
NC_000020.9:g.23590506T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+219T>G