Canonical Allele Identifier: CA2267413182
Gene:

Linked Data

dbSNP Id: rs2073474808

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788836G>T , CM000679.2:g.57788836G>T GRCh38
NC_000017.10:g.55866197G>T , CM000679.1:g.55866197G>T GRCh37
NC_000017.9:g.53221196G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16640C>A
XR_934881.3:n.3815-16640C>A