Canonical Allele Identifier: CA2734322457
Gene:

Linked Data

dbSNP Id: rs1968768098

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321238T>C , CM000680.2:g.10321238T>C GRCh38
NC_000018.9:g.10321235T>C , CM000680.1:g.10321235T>C GRCh37
NC_000018.8:g.10311235T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+910A>G
XR_001753344.1:n.650+910A>G
XR_001753345.1:n.883A>G
XR_001753346.1:n.549+910A>G