Canonical Allele Identifier: CA2137107142
Gene:

Linked Data

dbSNP Id: rs1003100063

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417666C>A , CM000676.2:g.52417666C>A GRCh38
NC_000014.8:g.52884384C>A , CM000676.1:g.52884384C>A GRCh37
NC_000014.7:g.51954134C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3037G>T