Canonical Allele Identifier: CA403106924

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755097A>C (hg19) ; chr19:g.7690211A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690211A>C , CM000681.2:g.7690211A>C	GRCh38
NC_000019.9:g.7755097A>C , CM000681.1:g.7755097A>C	GRCh37
NC_000019.8:g.7661097A>C	NCBI36
NG_029554.1:g.16936T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.676T>G MANE Select	ENSP00000471974.1:p.Leu226Val
ENST00000346664.9:c.676T>G	ENSP00000264072.6:p.Leu226Val
ENST00000360067.8:c.673T>G	ENSP00000353178.4:p.Leu225Val
ENST00000597312.5:n.1201T>G
ENST00000597921.5:c.676T>G	ENSP00000471974.1:p.Leu226Val
ENST00000597934.1:n.1038T>G
ENST00000598803.5:n.1171T>G
NM_001207019.2:c.673T>G	NP_001193948.2:p.Leu225Val
NM_001220500.1:c.676T>G	NP_001207429.1:p.Leu226Val
NM_002002.4:c.676T>G	NP_001993.2:p.Leu226Val
XM_005272462.3:c.676T>G	XP_005272519.1:p.Leu226Val
XM_005272462.4:c.676T>G	XP_005272519.1:p.Leu226Val
NM_001220500.2:c.676T>G MANE Select	NP_001207429.1:p.Leu226Val
NM_001207019.3:c.673T>G	NP_001193948.2:p.Leu225Val
NM_002002.5:c.676T>G	NP_001993.2:p.Leu226Val