Canonical Allele Identifier: CA1586714357
Gene: HBEGF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333302G= , CM000667.2:g.140333302G= GRCh38
NC_000005.9:g.139712887G= , CM000667.1:g.139712887G= GRCh37
NC_000005.8:g.139693071G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*997C= MANE Select ENSP00000230990.6:n.*997C=
ENST00000230990.6:c.*997C= ENSP00000230990.6:n.*997C=
NM_001945.2:c.*997C= NP_001936.1:n.*997C=
NM_001945.3:c.*997C= MANE Select NP_001936.1:n.*997C=