Canonical Allele Identifier: CA2754235721

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216028778A>G , CM000664.2:g.216028778A>G GRCh38
NC_000002.11:g.216893501A>G , CM000664.1:g.216893501A>G GRCh37
NC_000002.10:g.216601746A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420348.1:c.-68+4011T>C (MREG) ENSP00000404470.1:n.-68+4011T>C
ENST00000424992.5:c.-68+5184T>C (MREG) ENSP00000413302.1:n.-68+5184T>C
ENST00000439791.5:c.-68+4905T>C (MREG) ENSP00000411076.1:n.-68+4905T>C
ENST00000442122.5:c.*440+10413T>C (PECR) ENSP00000395512.1:n.*440+10413T>C
NM_001372189.1:c.-68+5184T>C (MREG) NP_001359118.1:n.-68+5184T>C
NM_001372190.1:c.-68+4905T>C (MREG) NP_001359119.1:n.-68+4905T>C