Canonical Allele Identifier: CA1181633473
Gene:

Linked Data

dbSNP Id: rs1652357903

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564038C>T , CM000663.2:g.94564038C>T GRCh38
NC_000001.10:g.95029594C>T , CM000663.1:g.95029594C>T GRCh37
NC_000001.9:g.94802182C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+425C>T