Canonical Allele Identifier: CA1586714413
Gene: HBEGF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333370G= , CM000667.2:g.140333370G= GRCh38
NC_000005.9:g.139712955G= , CM000667.1:g.139712955G= GRCh37
NC_000005.8:g.139693139G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*929C= MANE Select ENSP00000230990.6:n.*929C=
ENST00000230990.6:c.*929C= ENSP00000230990.6:n.*929C=
NM_001945.2:c.*929C= NP_001936.1:n.*929C=
NM_001945.3:c.*929C= MANE Select NP_001936.1:n.*929C=
Search 100 bp 5'
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