Canonical Allele Identifier: CA2675573848
Gene: HBEGF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333301A>G , CM000667.2:g.140333301A>G GRCh38
NC_000005.9:g.139712886A>G , CM000667.1:g.139712886A>G GRCh37
NC_000005.8:g.139693070A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*998T>C MANE Select ENSP00000230990.6:n.*998T>C
ENST00000230990.6:c.*998T>C ENSP00000230990.6:n.*998T>C
NM_001945.2:c.*998T>C NP_001936.1:n.*998T>C
NM_001945.3:c.*998T>C MANE Select NP_001936.1:n.*998T>C