Canonical Allele Identifier: CA505230111

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755436C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690550C>G , CM000681.2:g.7690550C>G	GRCh38
NC_000019.9:g.7755436C>G , CM000681.1:g.7755436C>G	GRCh37
NC_000019.8:g.7661436C>G	NCBI36
NG_029554.1:g.16597G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.477G>C MANE Select	ENSP00000471974.1:p.Val159=
ENST00000346664.9:c.477G>C	ENSP00000264072.6:p.Val159=
ENST00000360067.8:c.474G>C	ENSP00000353178.4:p.Val158=
ENST00000593418.1:c.414G>C	ENSP00000472067.1:p.Val138=
ENST00000597312.5:n.1002G>C
ENST00000597921.5:c.477G>C	ENSP00000471974.1:p.Val159=
ENST00000597934.1:n.839G>C
ENST00000598803.5:n.972G>C
NM_001207019.2:c.474G>C	NP_001193948.2:p.Val158=
NM_001220500.1:c.477G>C	NP_001207429.1:p.Val159=
NM_002002.4:c.477G>C	NP_001993.2:p.Val159=
XM_005272462.3:c.477G>C	XP_005272519.1:p.Val159=
XM_005272462.4:c.477G>C	XP_005272519.1:p.Val159=
NM_001220500.2:c.477G>C MANE Select	NP_001207429.1:p.Val159=
NM_001207019.3:c.474G>C	NP_001193948.2:p.Val158=
NM_002002.5:c.477G>C	NP_001993.2:p.Val159=