Canonical Allele Identifier: CA403107125

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755110A>C (hg19) ; chr19:g.7690224A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690224A>C , CM000681.2:g.7690224A>C	GRCh38
NC_000019.9:g.7755110A>C , CM000681.1:g.7755110A>C	GRCh37
NC_000019.8:g.7661110A>C	NCBI36
NG_029554.1:g.16923T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.663T>G MANE Select	ENSP00000471974.1:p.Ile221Met
ENST00000346664.9:c.663T>G	ENSP00000264072.6:p.Ile221Met
ENST00000360067.8:c.660T>G	ENSP00000353178.4:p.Ile220Met
ENST00000597312.5:n.1188T>G
ENST00000597921.5:c.663T>G	ENSP00000471974.1:p.Ile221Met
ENST00000597934.1:n.1025T>G
ENST00000598803.5:n.1158T>G
NM_001207019.2:c.660T>G	NP_001193948.2:p.Ile220Met
NM_001220500.1:c.663T>G	NP_001207429.1:p.Ile221Met
NM_002002.4:c.663T>G	NP_001993.2:p.Ile221Met
XM_005272462.3:c.663T>G	XP_005272519.1:p.Ile221Met
XM_005272462.4:c.663T>G	XP_005272519.1:p.Ile221Met
NM_001220500.2:c.663T>G MANE Select	NP_001207429.1:p.Ile221Met
NM_001207019.3:c.660T>G	NP_001193948.2:p.Ile220Met
NM_002002.5:c.663T>G	NP_001993.2:p.Ile221Met