Canonical Allele Identifier: CA2321045795

Gene: FCER2

Linked Data

• dbSNP Id: rs2032818704
• gnomAD v4: 19-7690129-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690133del , CM000681.2:g.7690133del	GRCh38
NC_000019.9:g.7755019del , CM000681.1:g.7755019del	GRCh37
NC_000019.8:g.7661019del	NCBI36
NG_029554.1:g.17017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.728+29del MANE Select	ENSP00000471974.1:n.728+29del
ENST00000346664.9:c.728+29del	ENSP00000264072.6:n.728+29del
ENST00000360067.8:c.725+29del	ENSP00000353178.4:n.725+29del
ENST00000597312.5:n.1253+29del
ENST00000597921.5:c.728+29del	ENSP00000471974.1:n.728+29del
ENST00000597934.1:n.1090+29del
ENST00000598803.5:n.1223+29del
NM_001207019.2:c.725+29del	NP_001193948.2:n.725+29del
NM_001220500.1:c.728+29del	NP_001207429.1:n.728+29del
NM_002002.4:c.728+29del	NP_001993.2:n.728+29del
XM_005272462.3:c.728+29del	XP_005272519.1:n.728+29del
XM_005272462.4:c.728+29del	XP_005272519.1:n.728+29del
NM_001220500.2:c.728+29del MANE Select	NP_001207429.1:n.728+29del
NM_001207019.3:c.725+29del	NP_001193948.2:n.725+29del
NM_002002.5:c.728+29del	NP_001993.2:n.728+29del