Canonical Allele Identifier: CA2729881963
Gene:

Linked Data

dbSNP Id: rs1033969904

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92314664A>C , CM000676.2:g.92314664A>C GRCh38
NC_000014.8:g.92781008A>C , CM000676.1:g.92781008A>C GRCh37
NC_000014.7:g.91850761A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.132-582A>C