Canonical Allele Identifier: CA1899263448
Gene:

Linked Data

dbSNP Id: rs1839589064

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201625T>C , CM000672.2:g.30201625T>C GRCh38
NC_000010.10:g.30490554T>C , CM000672.1:g.30490554T>C GRCh37
NC_000010.9:g.30530560T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930791.1:n.1193-1862T>C
XR_930791.2:n.1449-1862T>C