Canonical Allele Identifier: CA2129379059
Gene:

Linked Data

dbSNP Id: rs1882061432

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384882C>G , CM000676.2:g.36384882C>G GRCh38
NC_000014.8:g.36854087C>G , CM000676.1:g.36854087C>G GRCh37
NC_000014.7:g.35923838C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12277C>G XP_011535730.1:n.319-12277C>G
XR_943756.1:n.358+23786C>G