Canonical Allele Identifier: CA1468603667
Gene:

Linked Data

dbSNP Id: rs548894390

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74304349G>A , CM000666.2:g.74304349G>A GRCh38
NC_000004.11:g.75170066G>A , CM000666.1:g.75170066G>A GRCh37
NC_000004.10:g.75388930G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938877.1:n.120-25571C>T
XR_938877.2:n.126-25571C>T