Canonical Allele Identifier: CA403109517

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755420C>A (hg19) ; chr19:g.7690534C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690534C>A , CM000681.2:g.7690534C>A	GRCh38
NC_000019.9:g.7755420C>A , CM000681.1:g.7755420C>A	GRCh37
NC_000019.8:g.7661420C>A	NCBI36
NG_029554.1:g.16613G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.493G>T MANE Select	ENSP00000471974.1:p.Glu165Ter
ENST00000346664.9:c.493G>T	ENSP00000264072.6:p.Glu165Ter
ENST00000360067.8:c.490G>T	ENSP00000353178.4:p.Glu164Ter
ENST00000593418.1:c.430G>T	ENSP00000472067.1:p.Glu144Ter
ENST00000597312.5:n.1018G>T
ENST00000597921.5:c.493G>T	ENSP00000471974.1:p.Glu165Ter
ENST00000597934.1:n.855G>T
ENST00000598803.5:n.988G>T
NM_001207019.2:c.490G>T	NP_001193948.2:p.Glu164Ter
NM_001220500.1:c.493G>T	NP_001207429.1:p.Glu165Ter
NM_002002.4:c.493G>T	NP_001993.2:p.Glu165Ter
XM_005272462.3:c.493G>T	XP_005272519.1:p.Glu165Ter
XM_005272462.4:c.493G>T	XP_005272519.1:p.Glu165Ter
NM_001220500.2:c.493G>T MANE Select	NP_001207429.1:p.Glu165Ter
NM_001207019.3:c.490G>T	NP_001193948.2:p.Glu164Ter
NM_002002.5:c.493G>T	NP_001993.2:p.Glu165Ter