Canonical Allele Identifier: CA403107102

Gene: FCER2

Linked Data

• dbSNP Id: rs1274154825
• gnomAD v2: 19-7755109-C-T
• gnomAD v4: 19-7690223-C-T
• MyVariant Identifiers: chr19:g.7755109C>T (hg19) ; chr19:g.7690223C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690223C>T , CM000681.2:g.7690223C>T	GRCh38
NC_000019.9:g.7755109C>T , CM000681.1:g.7755109C>T	GRCh37
NC_000019.8:g.7661109C>T	NCBI36
NG_029554.1:g.16924G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000597921.6:c.664G>A MANE Select	ENSP00000471974.1:p.Gly222Ser
ENST00000346664.9:c.664G>A	ENSP00000264072.6:p.Gly222Ser
ENST00000360067.8:c.661G>A	ENSP00000353178.4:p.Gly221Ser
ENST00000597312.5:n.1189G>A
ENST00000597921.5:c.664G>A	ENSP00000471974.1:p.Gly222Ser
ENST00000597934.1:n.1026G>A
ENST00000598803.5:n.1159G>A
NM_001207019.2:c.661G>A	NP_001193948.2:p.Gly221Ser
NM_001220500.1:c.664G>A	NP_001207429.1:p.Gly222Ser
NM_002002.4:c.664G>A	NP_001993.2:p.Gly222Ser
XM_005272462.3:c.664G>A	XP_005272519.1:p.Gly222Ser
XM_005272462.4:c.664G>A	XP_005272519.1:p.Gly222Ser
NM_001220500.2:c.664G>A MANE Select	NP_001207429.1:p.Gly222Ser
NM_001207019.3:c.661G>A	NP_001193948.2:p.Gly221Ser
NM_002002.5:c.664G>A	NP_001993.2:p.Gly222Ser