Canonical Allele Identifier: CA2321046052

Gene: FCER2

Linked Data

• dbSNP Id: rs778619621

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690598T>G , CM000681.2:g.7690598T>G	GRCh38
NC_000019.9:g.7755484T>G , CM000681.1:g.7755484T>G	GRCh37
NC_000019.8:g.7661484T>G	NCBI36
NG_029554.1:g.16549A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-41A>C MANE Select	ENSP00000471974.1:n.470-41A>C
ENST00000346664.9:c.470-41A>C	ENSP00000264072.6:n.470-41A>C
ENST00000360067.8:c.467-41A>C	ENSP00000353178.4:n.467-41A>C
ENST00000593418.1:c.407-41A>C	ENSP00000472067.1:n.407-41A>C
ENST00000597312.5:n.995-41A>C
ENST00000597921.5:c.470-41A>C	ENSP00000471974.1:n.470-41A>C
ENST00000597934.1:n.832-41A>C
ENST00000598803.5:n.965-41A>C
NM_001207019.2:c.467-41A>C	NP_001193948.2:n.467-41A>C
NM_001220500.1:c.470-41A>C	NP_001207429.1:n.470-41A>C
NM_002002.4:c.470-41A>C	NP_001993.2:n.470-41A>C
XM_005272462.3:c.470-41A>C	XP_005272519.1:n.470-41A>C
XM_005272462.4:c.470-41A>C	XP_005272519.1:n.470-41A>C
NM_001220500.2:c.470-41A>C MANE Select	NP_001207429.1:n.470-41A>C
NM_001207019.3:c.467-41A>C	NP_001193948.2:n.467-41A>C
NM_002002.5:c.470-41A>C	NP_001993.2:n.470-41A>C