Canonical Allele Identifier: CA2267413203
Gene:

Linked Data

dbSNP Id: rs2073475138

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788898A>G , CM000679.2:g.57788898A>G GRCh38
NC_000017.10:g.55866259A>G , CM000679.1:g.55866259A>G GRCh37
NC_000017.9:g.53221258A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16702T>C
XR_934881.3:n.3815-16702T>C