Canonical Allele Identifier: CA505404858

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755103G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690217G>T , CM000681.2:g.7690217G>T	GRCh38
NC_000019.9:g.7755103G>T , CM000681.1:g.7755103G>T	GRCh37
NC_000019.8:g.7661103G>T	NCBI36
NG_029554.1:g.16930C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.670C>A MANE Select	ENSP00000471974.1:p.Arg224=
ENST00000346664.9:c.670C>A	ENSP00000264072.6:p.Arg224=
ENST00000360067.8:c.667C>A	ENSP00000353178.4:p.Arg223=
ENST00000597312.5:n.1195C>A
ENST00000597921.5:c.670C>A	ENSP00000471974.1:p.Arg224=
ENST00000597934.1:n.1032C>A
ENST00000598803.5:n.1165C>A
NM_001207019.2:c.667C>A	NP_001193948.2:p.Arg223=
NM_001220500.1:c.670C>A	NP_001207429.1:p.Arg224=
NM_002002.4:c.670C>A	NP_001993.2:p.Arg224=
XM_005272462.3:c.670C>A	XP_005272519.1:p.Arg224=
XM_005272462.4:c.670C>A	XP_005272519.1:p.Arg224=
NM_001220500.2:c.670C>A MANE Select	NP_001207429.1:p.Arg224=
NM_001207019.3:c.667C>A	NP_001193948.2:p.Arg223=
NM_002002.5:c.670C>A	NP_001993.2:p.Arg224=