Canonical Allele Identifier: CA2386425906
Gene:

Linked Data

dbSNP Id: rs1162100873

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32890287C>T , CM000683.2:g.32890287C>T GRCh38
NC_000021.8:g.34262595C>T , CM000683.1:g.34262595C>T GRCh37
NC_000021.7:g.33184465C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937669.1:n.460-3291C>T
XR_937669.2:n.1038-3291C>T