Canonical Allele Identifier: CA2717992000
Gene:

Linked Data

dbSNP Id: rs2130730658

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269604C>T , CM000670.2:g.97269604C>T GRCh38
NC_000008.10:g.98281832C>T , CM000670.1:g.98281832C>T GRCh37
NC_000008.9:g.98351008C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149466G>A