Canonical Allele Identifier: CA403108597

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755338T>G (hg19) ; chr19:g.7690452T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690452T>G , CM000681.2:g.7690452T>G	GRCh38
NC_000019.9:g.7755338T>G , CM000681.1:g.7755338T>G	GRCh37
NC_000019.8:g.7661338T>G	NCBI36
NG_029554.1:g.16695A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.575A>C MANE Select	ENSP00000471974.1:p.Asp192Ala
ENST00000346664.9:c.575A>C	ENSP00000264072.6:p.Asp192Ala
ENST00000360067.8:c.572A>C	ENSP00000353178.4:p.Asp191Ala
ENST00000597312.5:n.1100A>C
ENST00000597921.5:c.575A>C	ENSP00000471974.1:p.Asp192Ala
ENST00000597934.1:n.937A>C
ENST00000598803.5:n.1070A>C
NM_001207019.2:c.572A>C	NP_001193948.2:p.Asp191Ala
NM_001220500.1:c.575A>C	NP_001207429.1:p.Asp192Ala
NM_002002.4:c.575A>C	NP_001993.2:p.Asp192Ala
XM_005272462.3:c.575A>C	XP_005272519.1:p.Asp192Ala
XM_005272462.4:c.575A>C	XP_005272519.1:p.Asp192Ala
NM_001220500.2:c.575A>C MANE Select	NP_001207429.1:p.Asp192Ala
NM_001207019.3:c.572A>C	NP_001193948.2:p.Asp191Ala
NM_002002.5:c.575A>C	NP_001993.2:p.Asp192Ala