Canonical Allele Identifier: CA1327644349

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033843G= , CM000664.2:g.216033843G= GRCh38
NC_000002.11:g.216898566G= , CM000664.1:g.216898566G= GRCh37
NC_000002.10:g.216606811G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000424992.5:c.-68+119C= (MREG) ENSP00000413302.1:n.-68+119C=
ENST00000442122.5:c.*440+5348C= (PECR) ENSP00000395512.1:n.*440+5348C=
XR_001738847.2:n.1056-991C= (PECR)
NM_001372189.1:c.-68+119C= (MREG) NP_001359118.1:n.-68+119C=