Canonical Allele Identifier: CA1284431879
Gene:

Linked Data

dbSNP Id: rs1678953868

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369296C>G , CM000664.2:g.122369296C>G GRCh38
NC_000002.11:g.123126872C>G , CM000664.1:g.123126872C>G GRCh37
NC_000002.10:g.122843342C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23667C>G
XR_001739684.1:n.556-23667C>G