Canonical Allele Identifier: CA2729900808
Gene:

Linked Data

dbSNP Id: rs1410051075

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307357C>G , CM000676.2:g.92307357C>G GRCh38
NC_000014.8:g.92773701C>G , CM000676.1:g.92773701C>G GRCh37
NC_000014.7:g.91843454C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2813C>G