Canonical Allele Identifier: CA1327644395

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033957C= , CM000664.2:g.216033957C= GRCh38
NC_000002.11:g.216898680C= , CM000664.1:g.216898680C= GRCh37
NC_000002.10:g.216606925C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000424992.5:c.-68+5G= (MREG) ENSP00000413302.1:n.-68+5G=
ENST00000442122.5:c.*440+5234G= (PECR) ENSP00000395512.1:n.*440+5234G=
XR_001738847.2:n.1056-1105G= (PECR)
NM_001372189.1:c.-68+5G= (MREG) NP_001359118.1:n.-68+5G=