Canonical Allele Identifier: CA2587988682

Gene: FCER2

Linked Data

• gnomAD v4: 19-7690033-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690033T>G , CM000681.2:g.7690033T>G	GRCh38
NC_000019.9:g.7754919T>G , CM000681.1:g.7754919T>G	GRCh37
NC_000019.8:g.7660919T>G	NCBI36
NG_029554.1:g.17114A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.728+126A>C MANE Select	ENSP00000471974.1:n.728+126A>C
ENST00000346664.9:c.728+126A>C	ENSP00000264072.6:n.728+126A>C
ENST00000360067.8:c.725+126A>C	ENSP00000353178.4:n.725+126A>C
ENST00000597312.5:n.1253+126A>C
ENST00000597921.5:c.728+126A>C	ENSP00000471974.1:n.728+126A>C
ENST00000597934.1:n.1090+126A>C
ENST00000598803.5:n.1223+126A>C
NM_001207019.2:c.725+126A>C	NP_001193948.2:n.725+126A>C
NM_001220500.1:c.728+126A>C	NP_001207429.1:n.728+126A>C
NM_002002.4:c.728+126A>C	NP_001993.2:n.728+126A>C
XM_005272462.3:c.728+126A>C	XP_005272519.1:n.728+126A>C
XM_005272462.4:c.728+126A>C	XP_005272519.1:n.728+126A>C
NM_001220500.2:c.728+126A>C MANE Select	NP_001207429.1:n.728+126A>C
NM_001207019.3:c.725+126A>C	NP_001193948.2:n.725+126A>C
NM_002002.5:c.728+126A>C	NP_001993.2:n.728+126A>C