Canonical Allele Identifier: CA2321046029

Gene: FCER2

Linked Data

• dbSNP Id: rs2277995
• gnomAD v4: 19-7690583-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690583T>A , CM000681.2:g.7690583T>A	GRCh38
NC_000019.9:g.7755469T>A , CM000681.1:g.7755469T>A	GRCh37
NC_000019.8:g.7661469T>A	NCBI36
NG_029554.1:g.16564A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-26A>T MANE Select	ENSP00000471974.1:n.470-26A>T
ENST00000346664.9:c.470-26A>T	ENSP00000264072.6:n.470-26A>T
ENST00000360067.8:c.467-26A>T	ENSP00000353178.4:n.467-26A>T
ENST00000593418.1:c.407-26A>T	ENSP00000472067.1:n.407-26A>T
ENST00000597312.5:n.995-26A>T
ENST00000597921.5:c.470-26A>T	ENSP00000471974.1:n.470-26A>T
ENST00000597934.1:n.832-26A>T
ENST00000598803.5:n.965-26A>T
NM_001207019.2:c.467-26A>T	NP_001193948.2:n.467-26A>T
NM_001220500.1:c.470-26A>T	NP_001207429.1:n.470-26A>T
NM_002002.4:c.470-26A>T	NP_001993.2:n.470-26A>T
XM_005272462.3:c.470-26A>T	XP_005272519.1:n.470-26A>T
XM_005272462.4:c.470-26A>T	XP_005272519.1:n.470-26A>T
NM_001220500.2:c.470-26A>T MANE Select	NP_001207429.1:n.470-26A>T
NM_001207019.3:c.467-26A>T	NP_001193948.2:n.467-26A>T
NM_002002.5:c.470-26A>T	NP_001993.2:n.470-26A>T