Canonical Allele Identifier: CA2263926945
Gene:

Linked Data

dbSNP Id: rs1908569906

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211765A>C , CM000679.2:g.50211765A>C GRCh38
NC_000017.10:g.48289126A>C , CM000679.1:g.48289126A>C GRCh37
NC_000017.9:g.45644125A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934838.1:n.43-2070A>C