Canonical Allele Identifier: CA505405180

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755409G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690523G>A , CM000681.2:g.7690523G>A	GRCh38
NC_000019.9:g.7755409G>A , CM000681.1:g.7755409G>A	GRCh37
NC_000019.8:g.7661409G>A	NCBI36
NG_029554.1:g.16624C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.504C>T MANE Select	ENSP00000471974.1:p.Ile168=
ENST00000346664.9:c.504C>T	ENSP00000264072.6:p.Ile168=
ENST00000360067.8:c.501C>T	ENSP00000353178.4:p.Ile167=
ENST00000593418.1:c.441C>T	ENSP00000472067.1:p.Ile147=
ENST00000597312.5:n.1029C>T
ENST00000597921.5:c.504C>T	ENSP00000471974.1:p.Ile168=
ENST00000597934.1:n.866C>T
ENST00000598803.5:n.999C>T
NM_001207019.2:c.501C>T	NP_001193948.2:p.Ile167=
NM_001220500.1:c.504C>T	NP_001207429.1:p.Ile168=
NM_002002.4:c.504C>T	NP_001993.2:p.Ile168=
XM_005272462.3:c.504C>T	XP_005272519.1:p.Ile168=
XM_005272462.4:c.504C>T	XP_005272519.1:p.Ile168=
NM_001220500.2:c.504C>T MANE Select	NP_001207429.1:p.Ile168=
NM_001207019.3:c.501C>T	NP_001193948.2:p.Ile167=
NM_002002.5:c.504C>T	NP_001993.2:p.Ile168=