Canonical Allele Identifier: CA1586714112
Gene: HBEGF HGNC NCBI

Linked Data

dbSNP Id: rs7268
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140332965A>T , CM000667.2:g.140332965A>T GRCh38
NC_000005.9:g.139712550A>T , CM000667.1:g.139712550A>T GRCh37
NC_000005.8:g.139692734A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*1334T>A MANE Select ENSP00000230990.6:n.*1334T>A
ENST00000230990.6:c.*1334T>A ENSP00000230990.6:n.*1334T>A
NM_001945.2:c.*1334T>A NP_001936.1:n.*1334T>A
NM_001945.3:c.*1334T>A MANE Select NP_001936.1:n.*1334T>A
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