Canonical Allele Identifier: CA2267413185
Gene:

Linked Data

dbSNP Id: rs2073474823

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788841A>G , CM000679.2:g.57788841A>G GRCh38
NC_000017.10:g.55866202A>G , CM000679.1:g.55866202A>G GRCh37
NC_000017.9:g.53221201A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16645T>C
XR_934881.3:n.3815-16645T>C