Canonical Allele Identifier: CA403109387

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755406A>T (hg19) ; chr19:g.7690520A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690520A>T , CM000681.2:g.7690520A>T	GRCh38
NC_000019.9:g.7755406A>T , CM000681.1:g.7755406A>T	GRCh37
NC_000019.8:g.7661406A>T	NCBI36
NG_029554.1:g.16627T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.507T>A MANE Select	ENSP00000471974.1:p.Asn169Lys
ENST00000346664.9:c.507T>A	ENSP00000264072.6:p.Asn169Lys
ENST00000360067.8:c.504T>A	ENSP00000353178.4:p.Asn168Lys
ENST00000593418.1:c.444T>A	ENSP00000472067.1:p.Asn148Lys
ENST00000597312.5:n.1032T>A
ENST00000597921.5:c.507T>A	ENSP00000471974.1:p.Asn169Lys
ENST00000597934.1:n.869T>A
ENST00000598803.5:n.1002T>A
NM_001207019.2:c.504T>A	NP_001193948.2:p.Asn168Lys
NM_001220500.1:c.507T>A	NP_001207429.1:p.Asn169Lys
NM_002002.4:c.507T>A	NP_001993.2:p.Asn169Lys
XM_005272462.3:c.507T>A	XP_005272519.1:p.Asn169Lys
XM_005272462.4:c.507T>A	XP_005272519.1:p.Asn169Lys
NM_001220500.2:c.507T>A MANE Select	NP_001207429.1:p.Asn169Lys
NM_001207019.3:c.504T>A	NP_001193948.2:p.Asn168Lys
NM_002002.5:c.507T>A	NP_001993.2:p.Asn169Lys