Canonical Allele Identifier: CA2663016676

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033746G>A , CM000664.2:g.216033746G>A GRCh38
NC_000002.11:g.216898469G>A , CM000664.1:g.216898469G>A GRCh37
NC_000002.10:g.216606714G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000424992.5:c.-68+216C>T (MREG) ENSP00000413302.1:n.-68+216C>T
ENST00000439791.5:c.-131C>T (MREG) ENSP00000411076.1:n.-131C>T
ENST00000442122.5:c.*440+5445C>T (PECR) ENSP00000395512.1:n.*440+5445C>T
XR_001738847.2:n.1056-894C>T (PECR)
NM_001372189.1:c.-68+216C>T (MREG) NP_001359118.1:n.-68+216C>T
NM_001372190.1:c.-131C>T (MREG) NP_001359119.1:n.-131C>T