Canonical Allele Identifier: CA1586714372
Gene: HBEGF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333323T= , CM000667.2:g.140333323T= GRCh38
NC_000005.9:g.139712908T= , CM000667.1:g.139712908T= GRCh37
NC_000005.8:g.139693092T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*976A= MANE Select ENSP00000230990.6:n.*976A=
ENST00000230990.6:c.*976A= ENSP00000230990.6:n.*976A=
NM_001945.2:c.*976A= NP_001936.1:n.*976A=
NM_001945.3:c.*976A= MANE Select NP_001936.1:n.*976A=
Search 100 bp 5'
Search 100 bp 3'