Canonical Allele Identifier: CA505230120

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755442G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690556G>C , CM000681.2:g.7690556G>C	GRCh38
NC_000019.9:g.7755442G>C , CM000681.1:g.7755442G>C	GRCh37
NC_000019.8:g.7661442G>C	NCBI36
NG_029554.1:g.16591C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.471C>G MANE Select	ENSP00000471974.1:p.Gly157=
ENST00000346664.9:c.471C>G	ENSP00000264072.6:p.Gly157=
ENST00000360067.8:c.468C>G	ENSP00000353178.4:p.Gly156=
ENST00000593418.1:c.408C>G	ENSP00000472067.1:p.Gly136=
ENST00000597312.5:n.996C>G
ENST00000597921.5:c.471C>G	ENSP00000471974.1:p.Gly157=
ENST00000597934.1:n.833C>G
ENST00000598803.5:n.966C>G
NM_001207019.2:c.468C>G	NP_001193948.2:p.Gly156=
NM_001220500.1:c.471C>G	NP_001207429.1:p.Gly157=
NM_002002.4:c.471C>G	NP_001993.2:p.Gly157=
XM_005272462.3:c.471C>G	XP_005272519.1:p.Gly157=
XM_005272462.4:c.471C>G	XP_005272519.1:p.Gly157=
NM_001220500.2:c.471C>G MANE Select	NP_001207429.1:p.Gly157=
NM_001207019.3:c.468C>G	NP_001193948.2:p.Gly156=
NM_002002.5:c.471C>G	NP_001993.2:p.Gly157=