Canonical Allele Identifier: CA2729743233
Gene:

Linked Data

dbSNP Id: rs2140087143

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417639T>C , CM000676.2:g.52417639T>C GRCh38
NC_000014.8:g.52884357T>C , CM000676.1:g.52884357T>C GRCh37
NC_000014.7:g.51954107T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3064A>G