Canonical Allele Identifier: CA2663016770

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033986T>C , CM000664.2:g.216033986T>C GRCh38
NC_000002.11:g.216898709T>C , CM000664.1:g.216898709T>C GRCh37
NC_000002.10:g.216606954T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424992.5:c.-92A>G (MREG) ENSP00000413302.1:n.-92A>G
ENST00000442122.5:c.*440+5205A>G (PECR) ENSP00000395512.1:n.*440+5205A>G
XR_001738847.2:n.1056-1134A>G (PECR)
NM_001372189.1:c.-92A>G (MREG) NP_001359118.1:n.-92A>G