Canonical Allele Identifier: CA2002576384
Gene:

Linked Data

dbSNP Id: rs1861335890

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116442796A>G , CM000673.2:g.116442796A>G GRCh38
NC_000011.9:g.116313513A>G , CM000673.1:g.116313513A>G GRCh37
NC_000011.8:g.115818723A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748403.1:n.349+31081T>C