Canonical Allele Identifier: CA2675573560
Gene: HBEGF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140332944A>G , CM000667.2:g.140332944A>G GRCh38
NC_000005.9:g.139712529A>G , CM000667.1:g.139712529A>G GRCh37
NC_000005.8:g.139692713A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*1355T>C MANE Select ENSP00000230990.6:n.*1355T>C
ENST00000230990.6:c.*1355T>C ENSP00000230990.6:n.*1355T>C
NM_001945.2:c.*1355T>C NP_001936.1:n.*1355T>C
NM_001945.3:c.*1355T>C MANE Select NP_001936.1:n.*1355T>C