Canonical Allele Identifier: CA1042294375

Linked Data

dbSNP Id: rs1694751802

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033940C>A , CM000664.2:g.216033940C>A GRCh38
NC_000002.11:g.216898663C>A , CM000664.1:g.216898663C>A GRCh37
NC_000002.10:g.216606908C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000424992.5:c.-68+22G>T (MREG) ENSP00000413302.1:n.-68+22G>T
ENST00000442122.5:c.*440+5251G>T (PECR) ENSP00000395512.1:n.*440+5251G>T
XR_001738847.2:n.1056-1088G>T (PECR)
NM_001372189.1:c.-68+22G>T (MREG) NP_001359118.1:n.-68+22G>T