Canonical Allele Identifier: CA1586714524
Gene: HBEGF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333511A= , CM000667.2:g.140333511A= GRCh38
NC_000005.9:g.139713096A= , CM000667.1:g.139713096A= GRCh37
NC_000005.8:g.139693280A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*788T= MANE Select ENSP00000230990.6:n.*788T=
ENST00000230990.6:c.*788T= ENSP00000230990.6:n.*788T=
NM_001945.2:c.*788T= NP_001936.1:n.*788T=
NM_001945.3:c.*788T= MANE Select NP_001936.1:n.*788T=