Canonical Allele Identifier: CA2717991997
Gene:

Linked Data

dbSNP Id: rs2130730643

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269574G>T , CM000670.2:g.97269574G>T GRCh38
NC_000008.10:g.98281802G>T , CM000670.1:g.98281802G>T GRCh37
NC_000008.9:g.98350978G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149496C>A