Canonical Allele Identifier: CA403109010

Gene: FCER2

Linked Data

• gnomAD v4: 19-7690489-C-T
• MyVariant Identifiers: chr19:g.7755375C>T (hg19) ; chr19:g.7690489C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690489C>T , CM000681.2:g.7690489C>T	GRCh38
NC_000019.9:g.7755375C>T , CM000681.1:g.7755375C>T	GRCh37
NC_000019.8:g.7661375C>T	NCBI36
NG_029554.1:g.16658G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.538G>A MANE Select	ENSP00000471974.1:p.Gly180Ser
ENST00000346664.9:c.538G>A	ENSP00000264072.6:p.Gly180Ser
ENST00000360067.8:c.535G>A	ENSP00000353178.4:p.Gly179Ser
ENST00000593418.1:c.475G>A	ENSP00000472067.1:p.Gly159Ser
ENST00000597312.5:n.1063G>A
ENST00000597921.5:c.538G>A	ENSP00000471974.1:p.Gly180Ser
ENST00000597934.1:n.900G>A
ENST00000598803.5:n.1033G>A
NM_001207019.2:c.535G>A	NP_001193948.2:p.Gly179Ser
NM_001220500.1:c.538G>A	NP_001207429.1:p.Gly180Ser
NM_002002.4:c.538G>A	NP_001993.2:p.Gly180Ser
XM_005272462.3:c.538G>A	XP_005272519.1:p.Gly180Ser
XM_005272462.4:c.538G>A	XP_005272519.1:p.Gly180Ser
NM_001220500.2:c.538G>A MANE Select	NP_001207429.1:p.Gly180Ser
NM_001207019.3:c.535G>A	NP_001193948.2:p.Gly179Ser
NM_002002.5:c.538G>A	NP_001993.2:p.Gly180Ser