Canonical Allele Identifier: CA2675573881
Gene: HBEGF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333332C>A , CM000667.2:g.140333332C>A GRCh38
NC_000005.9:g.139712917C>A , CM000667.1:g.139712917C>A GRCh37
NC_000005.8:g.139693101C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*967G>T MANE Select ENSP00000230990.6:n.*967G>T
ENST00000230990.6:c.*967G>T ENSP00000230990.6:n.*967G>T
NM_001945.2:c.*967G>T NP_001936.1:n.*967G>T
NM_001945.3:c.*967G>T MANE Select NP_001936.1:n.*967G>T