Canonical Allele Identifier: CA9144958

Gene: FCER2

Linked Data

• dbSNP Id: rs558619258
• ExAC: 19:7755115 A / G
• gnomAD v2: 19-7755115-A-G
• gnomAD v3: 19-7690229-A-G
• gnomAD v4: 19-7690229-A-G
• MyVariant Identifiers: chr19:g.7755115A>G (hg19) ; chr19:g.7690229A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690229A>G , CM000681.2:g.7690229A>G	GRCh38
NC_000019.9:g.7755115A>G , CM000681.1:g.7755115A>G	GRCh37
NC_000019.8:g.7661115A>G	NCBI36
NG_029554.1:g.16918T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.658T>C MANE Select	ENSP00000471974.1:p.Trp220Arg
ENST00000346664.9:c.658T>C	ENSP00000264072.6:p.Trp220Arg
ENST00000360067.8:c.655T>C	ENSP00000353178.4:p.Trp219Arg
ENST00000597312.5:n.1183T>C
ENST00000597921.5:c.658T>C	ENSP00000471974.1:p.Trp220Arg
ENST00000597934.1:n.1020T>C
ENST00000598803.5:n.1153T>C
NM_001207019.2:c.655T>C	NP_001193948.2:p.Trp219Arg
NM_001220500.1:c.658T>C	NP_001207429.1:p.Trp220Arg
NM_002002.4:c.658T>C	NP_001993.2:p.Trp220Arg
XM_005272462.3:c.658T>C	XP_005272519.1:p.Trp220Arg
XM_005272462.4:c.658T>C	XP_005272519.1:p.Trp220Arg
NM_001220500.2:c.658T>C MANE Select	NP_001207429.1:p.Trp220Arg
NM_001207019.3:c.655T>C	NP_001193948.2:p.Trp219Arg
NM_002002.5:c.658T>C	NP_001993.2:p.Trp220Arg