Canonical Allele Identifier: CA480366754

Gene: ERBB3

Linked Data

• dbSNP Id: rs2136795224
• MyVariant Identifiers: chr12:g.56481864C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56088080C>T , CM000674.2:g.56088080C>T	GRCh38
NC_000012.11:g.56481864C>T , CM000674.1:g.56481864C>T	GRCh37
NC_000012.10:g.54768131C>T	NCBI36
NG_011529.1:g.12973C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.951C>T
ENST00000683018.1:c.615C>T	ENSP00000506822.1:p.Val205=
ENST00000683059.1:c.615C>T	ENSP00000507402.1:p.Val205=
ENST00000683164.1:c.615C>T	ENSP00000508051.1:p.Val205=
ENST00000683653.1:n.746C>T
ENST00000684500.1:n.921C>T
ENST00000267101.8:c.792C>T MANE Select	ENSP00000267101.4:p.Val264=
ENST00000267101.7:c.792C>T	ENSP00000267101.3:p.Val264=
ENST00000415288.6:c.615C>T	ENSP00000408340.2:p.Val205=
ENST00000546748.1:n.257C>T
ENST00000550869.5:c.25-6401C>T	ENSP00000448671.1:n.25-6401C>T
ENST00000551085.5:c.792C>T	ENSP00000448483.1:p.Val264=
ENST00000551242.5:c.792C>T	ENSP00000447510.1:p.Val264=
NM_001982.3:c.792C>T	NP_001973.2:p.Val264=
NM_001982.4:c.792C>T MANE Select	NP_001973.2:p.Val264=