Canonical Allele Identifier: CA1586714289
Gene: HBEGF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333204A= , CM000667.2:g.140333204A= GRCh38
NC_000005.9:g.139712789A= , CM000667.1:g.139712789A= GRCh37
NC_000005.8:g.139692973A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*1095T= MANE Select ENSP00000230990.6:n.*1095T=
ENST00000230990.6:c.*1095T= ENSP00000230990.6:n.*1095T=
NM_001945.2:c.*1095T= NP_001936.1:n.*1095T=
NM_001945.3:c.*1095T= MANE Select NP_001936.1:n.*1095T=