Canonical Allele Identifier: CA2267413208
Gene:

Linked Data

dbSNP Id: rs2073475173

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788910G>C , CM000679.2:g.57788910G>C GRCh38
NC_000017.10:g.55866271G>C , CM000679.1:g.55866271G>C GRCh37
NC_000017.9:g.53221270G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16714C>G
XR_934881.3:n.3815-16714C>G