Canonical Allele Identifier: CA2267413200
Gene:

Linked Data

dbSNP Id: rs2073475020

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788895T>C , CM000679.2:g.57788895T>C GRCh38
NC_000017.10:g.55866256T>C , CM000679.1:g.55866256T>C GRCh37
NC_000017.9:g.53221255T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16699A>G
XR_934881.3:n.3815-16699A>G