Canonical Allele Identifier: CA2137107124
Gene:

Linked Data

dbSNP Id: rs2034713604

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417655G>C , CM000676.2:g.52417655G>C GRCh38
NC_000014.8:g.52884373G>C , CM000676.1:g.52884373G>C GRCh37
NC_000014.7:g.51954123G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3048C>G