Canonical Allele Identifier: CA1586714520
Gene: HBEGF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333506C= , CM000667.2:g.140333506C= GRCh38
NC_000005.9:g.139713091C= , CM000667.1:g.139713091C= GRCh37
NC_000005.8:g.139693275C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*793G= MANE Select ENSP00000230990.6:n.*793G=
ENST00000230990.6:c.*793G= ENSP00000230990.6:n.*793G=
NM_001945.2:c.*793G= NP_001936.1:n.*793G=
NM_001945.3:c.*793G= MANE Select NP_001936.1:n.*793G=