Canonical Allele Identifier: CA403107022

Gene: FCER2

Linked Data

• dbSNP Id: rs201998118
• gnomAD v2: 19-7755103-G-C
• gnomAD v4: 19-7690217-G-C
• MyVariant Identifiers: chr19:g.7755103G>C (hg19) ; chr19:g.7690217G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.670C>G MANE Select	ENSP00000471974.1:p.Arg224Gly
ENST00000346664.9:c.670C>G	ENSP00000264072.6:p.Arg224Gly
ENST00000360067.8:c.667C>G	ENSP00000353178.4:p.Arg223Gly
ENST00000597312.5:n.1195C>G
ENST00000597921.5:c.670C>G	ENSP00000471974.1:p.Arg224Gly
ENST00000597934.1:n.1032C>G
ENST00000598803.5:n.1165C>G
NM_001207019.2:c.667C>G	NP_001193948.2:p.Arg223Gly
NM_001220500.1:c.670C>G	NP_001207429.1:p.Arg224Gly
NM_002002.4:c.670C>G	NP_001993.2:p.Arg224Gly
XM_005272462.3:c.670C>G	XP_005272519.1:p.Arg224Gly
XM_005272462.4:c.670C>G	XP_005272519.1:p.Arg224Gly
NM_001220500.2:c.670C>G MANE Select	NP_001207429.1:p.Arg224Gly
NM_001207019.3:c.667C>G	NP_001193948.2:p.Arg223Gly
NM_002002.5:c.670C>G	NP_001993.2:p.Arg224Gly