Canonical Allele Identifier: CA1586714068
Gene: HBEGF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140332921C= , CM000667.2:g.140332921C= GRCh38
NC_000005.9:g.139712506C= , CM000667.1:g.139712506C= GRCh37
NC_000005.8:g.139692690C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*1378G= MANE Select ENSP00000230990.6:n.*1378G=
ENST00000230990.6:c.*1378G= ENSP00000230990.6:n.*1378G=
NM_001945.2:c.*1378G= NP_001936.1:n.*1378G=
NM_001945.3:c.*1378G= MANE Select NP_001936.1:n.*1378G=