Canonical Allele Identifier: CA1586714428
Gene: HBEGF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333389C= , CM000667.2:g.140333389C= GRCh38
NC_000005.9:g.139712974C= , CM000667.1:g.139712974C= GRCh37
NC_000005.8:g.139693158C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*910G= MANE Select ENSP00000230990.6:n.*910G=
ENST00000230990.6:c.*910G= ENSP00000230990.6:n.*910G=
NM_001945.2:c.*910G= NP_001936.1:n.*910G=
NM_001945.3:c.*910G= MANE Select NP_001936.1:n.*910G=
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