Canonical Allele Identifier: CA2619264226
Gene: ERBB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56087781C>T , CM000674.2:g.56087781C>T GRCh38
NC_000012.11:g.56481565C>T , CM000674.1:g.56481565C>T GRCh37
NC_000012.10:g.54767832C>T NCBI36
NG_011529.1:g.12674C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682431.1:n.773-14C>T
ENST00000683018.1:c.437-14C>T ENSP00000506822.1:n.437-14C>T
ENST00000683059.1:c.437-14C>T ENSP00000507402.1:n.437-14C>T
ENST00000683164.1:c.437-14C>T ENSP00000508051.1:n.437-14C>T
ENST00000683653.1:n.568-14C>T
ENST00000684500.1:n.743-14C>T
ENST00000267101.8:c.614-14C>T MANE Select ENSP00000267101.4:n.614-14C>T
ENST00000267101.7:c.614-14C>T ENSP00000267101.3:n.614-14C>T
ENST00000415288.6:c.437-14C>T ENSP00000408340.2:n.437-14C>T
ENST00000549472.1:n.343C>T
ENST00000550869.5:c.25-6700C>T ENSP00000448671.1:n.25-6700C>T
ENST00000551085.5:c.614-14C>T ENSP00000448483.1:n.614-14C>T
ENST00000551242.5:c.614-14C>T ENSP00000447510.1:n.614-14C>T
NM_001982.3:c.614-14C>T NP_001973.2:n.614-14C>T
NM_001982.4:c.614-14C>T MANE Select NP_001973.2:n.614-14C>T
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