Canonical Allele Identifier: CA1327644369
Gene: MREG HGNC NCBI
PECR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033895A= , CM000664.2:g.216033895A= GRCh38
NC_000002.11:g.216898618A= , CM000664.1:g.216898618A= GRCh37
NC_000002.10:g.216606863A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424992.5:c.-68+67T= (MREG) ENSP00000413302.1:n.-68+67T=
ENST00000442122.5:c.*440+5296T= (PECR) ENSP00000395512.1:n.*440+5296T=
XR_001738847.2:n.1056-1043T= (PECR)
NM_001372189.1:c.-68+67T= (MREG) NP_001359118.1:n.-68+67T=
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