Canonical Allele Identifier: CA182463539
Gene:

Linked Data

dbSNP Id: rs1008792042

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269581T>A , CM000670.2:g.97269581T>A GRCh38
NC_000008.10:g.98281809T>A , CM000670.1:g.98281809T>A GRCh37
NC_000008.9:g.98350985T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149489A>T