Canonical Allele Identifier: CA6622056

Gene: ERBB3

Linked Data

• dbSNP Id: rs771886822
• ExAC: 12:56481767 C / T
• gnomAD v2: 12-56481767-C-T
• gnomAD v4: 12-56087983-C-T
• MyVariant Identifiers: chr12:g.56481767C>T (hg19) ; chr12:g.56087983C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56087983C>T , CM000674.2:g.56087983C>T	GRCh38
NC_000012.11:g.56481767C>T , CM000674.1:g.56481767C>T	GRCh37
NC_000012.10:g.54768034C>T	NCBI36
NG_011529.1:g.12876C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682431.1:n.892-38C>T
ENST00000683018.1:c.556-38C>T	ENSP00000506822.1:n.556-38C>T
ENST00000683059.1:c.556-38C>T	ENSP00000507402.1:n.556-38C>T
ENST00000683164.1:c.556-38C>T	ENSP00000508051.1:n.556-38C>T
ENST00000683653.1:n.687-38C>T
ENST00000684500.1:n.862-38C>T
ENST00000267101.8:c.733-38C>T MANE Select	ENSP00000267101.4:n.733-38C>T
ENST00000267101.7:c.733-38C>T	ENSP00000267101.3:n.733-38C>T
ENST00000415288.6:c.556-38C>T	ENSP00000408340.2:n.556-38C>T
ENST00000546748.1:n.160C>T
ENST00000549472.1:n.476-38C>T
ENST00000550869.5:c.25-6498C>T	ENSP00000448671.1:n.25-6498C>T
ENST00000551085.5:c.733-38C>T	ENSP00000448483.1:n.733-38C>T
ENST00000551242.5:c.733-38C>T	ENSP00000447510.1:n.733-38C>T
NM_001982.3:c.733-38C>T	NP_001973.2:n.733-38C>T
NM_001982.4:c.733-38C>T MANE Select	NP_001973.2:n.733-38C>T