Canonical Allele Identifier: CA920050683

Gene: FCER2

Linked Data

• dbSNP Id: rs1599432061

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690589dup , CM000681.2:g.7690589dup	GRCh38
NC_000019.9:g.7755475dup , CM000681.1:g.7755475dup	GRCh37
NC_000019.8:g.7661475dup	NCBI36
NG_029554.1:g.16559dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-31dup MANE Select	ENSP00000471974.1:n.470-31dup
ENST00000346664.9:c.470-31dup	ENSP00000264072.6:n.470-31dup
ENST00000360067.8:c.467-31dup	ENSP00000353178.4:n.467-31dup
ENST00000593418.1:c.407-31dup	ENSP00000472067.1:n.407-31dup
ENST00000597312.5:n.995-31dup
ENST00000597921.5:c.470-31dup	ENSP00000471974.1:n.470-31dup
ENST00000597934.1:n.832-31dup
ENST00000598803.5:n.965-31dup
NM_001207019.2:c.467-31dup	NP_001193948.2:n.467-31dup
NM_001220500.1:c.470-31dup	NP_001207429.1:n.470-31dup
NM_002002.4:c.470-31dup	NP_001993.2:n.470-31dup
XM_005272462.3:c.470-31dup	XP_005272519.1:n.470-31dup
XM_005272462.4:c.470-31dup	XP_005272519.1:n.470-31dup
NM_001220500.2:c.470-31dup MANE Select	NP_001207429.1:n.470-31dup
NM_001207019.3:c.467-31dup	NP_001193948.2:n.467-31dup
NM_002002.5:c.470-31dup	NP_001993.2:n.470-31dup