Canonical Allele Identifier: CA529297684
Gene:

Linked Data

dbSNP Id: rs1257829773

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491633A>T , CM000663.2:g.220491633A>T GRCh38
NC_000001.10:g.220664975A>T , CM000663.1:g.220664975A>T GRCh37
NC_000001.9:g.218731598A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922615.1:n.256-601A>T
XR_001737822.1:n.557-601A>T