Canonical Allele Identifier: CA2129379065
Gene:

Linked Data

dbSNP Id: rs1882061654

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384893C>G , CM000676.2:g.36384893C>G GRCh38
NC_000014.8:g.36854098C>G , CM000676.1:g.36854098C>G GRCh37
NC_000014.7:g.35923849C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12266C>G XP_011535730.1:n.319-12266C>G
XR_943756.1:n.358+23797C>G