Canonical Allele Identifier: CA237619613
Gene: ERBB3 HGNC NCBI

Linked Data

dbSNP Id: rs1054701563

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56088328A>G , CM000674.2:g.56088328A>G GRCh38
NC_000012.11:g.56482112A>G , CM000674.1:g.56482112A>G GRCh37
NC_000012.10:g.54768379A>G NCBI36
NG_011529.1:g.13221A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682431.1:n.1033+166A>G
ENST00000683018.1:c.697+166A>G ENSP00000506822.1:n.697+166A>G
ENST00000683059.1:c.697+166A>G ENSP00000507402.1:n.697+166A>G
ENST00000683164.1:c.697+166A>G ENSP00000508051.1:n.697+166A>G
ENST00000683653.1:n.828+166A>G
ENST00000684500.1:n.1003+166A>G
ENST00000267101.8:c.874+166A>G MANE Select ENSP00000267101.4:n.874+166A>G
ENST00000267101.7:c.874+166A>G ENSP00000267101.3:n.874+166A>G
ENST00000415288.6:c.697+166A>G ENSP00000408340.2:n.697+166A>G
ENST00000546748.1:n.339+166A>G
ENST00000550869.5:c.25-6153A>G ENSP00000448671.1:n.25-6153A>G
ENST00000551085.5:c.874+166A>G ENSP00000448483.1:n.874+166A>G
ENST00000551242.5:c.874+166A>G ENSP00000447510.1:n.874+166A>G
NM_001982.3:c.874+166A>G NP_001973.2:n.874+166A>G
NM_001982.4:c.874+166A>G MANE Select NP_001973.2:n.874+166A>G