Canonical Allele Identifier: CA9144955

Gene: FCER2

Linked Data

• dbSNP Id: rs756205377
• ExAC: 19:7755102 C / T
• gnomAD v2: 19-7755102-C-T
• gnomAD v3: 19-7690216-C-T
• gnomAD v4: 19-7690216-C-T
• MyVariant Identifiers: chr19:g.7755102C>T (hg19) ; chr19:g.7690216C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690216C>T , CM000681.2:g.7690216C>T	GRCh38
NC_000019.9:g.7755102C>T , CM000681.1:g.7755102C>T	GRCh37
NC_000019.8:g.7661102C>T	NCBI36
NG_029554.1:g.16931G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000597921.6:c.671G>A MANE Select	ENSP00000471974.1:p.Arg224Gln
ENST00000346664.9:c.671G>A	ENSP00000264072.6:p.Arg224Gln
ENST00000360067.8:c.668G>A	ENSP00000353178.4:p.Arg223Gln
ENST00000597312.5:n.1196G>A
ENST00000597921.5:c.671G>A	ENSP00000471974.1:p.Arg224Gln
ENST00000597934.1:n.1033G>A
ENST00000598803.5:n.1166G>A
NM_001207019.2:c.668G>A	NP_001193948.2:p.Arg223Gln
NM_001220500.1:c.671G>A	NP_001207429.1:p.Arg224Gln
NM_002002.4:c.671G>A	NP_001993.2:p.Arg224Gln
XM_005272462.3:c.671G>A	XP_005272519.1:p.Arg224Gln
XM_005272462.4:c.671G>A	XP_005272519.1:p.Arg224Gln
NM_001220500.2:c.671G>A MANE Select	NP_001207429.1:p.Arg224Gln
NM_001207019.3:c.668G>A	NP_001193948.2:p.Arg223Gln
NM_002002.5:c.671G>A	NP_001993.2:p.Arg224Gln