Canonical Allele Identifier: CA2675573660
Gene: HBEGF HGNC NCBI

Linked Data

gnomAD v4: 5-140333123-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333123T>A , CM000667.2:g.140333123T>A GRCh38
NC_000005.9:g.139712708T>A , CM000667.1:g.139712708T>A GRCh37
NC_000005.8:g.139692892T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*1176A>T MANE Select ENSP00000230990.6:n.*1176A>T
ENST00000230990.6:c.*1176A>T ENSP00000230990.6:n.*1176A>T
NM_001945.2:c.*1176A>T NP_001936.1:n.*1176A>T
NM_001945.3:c.*1176A>T MANE Select NP_001936.1:n.*1176A>T
Search 100 bp 5'
Search 100 bp 3'