Canonical Allele Identifier: CA884237366

Gene: FCER2

Linked Data

• dbSNP Id: rs1461954973
• gnomAD v3: 19-7689950-C-T
• gnomAD v4: 19-7689950-C-T
• MyVariant Identifiers: chr19:g.7754836C>T (hg19) ; chr19:g.7689950C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7689950C>T , CM000681.2:g.7689950C>T	GRCh38
NC_000019.9:g.7754836C>T , CM000681.1:g.7754836C>T	GRCh37
NC_000019.8:g.7660836C>T	NCBI36
NG_029554.1:g.17197G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.728+209G>A MANE Select	ENSP00000471974.1:n.728+209G>A
ENST00000346664.9:c.728+209G>A	ENSP00000264072.6:n.728+209G>A
ENST00000360067.8:c.725+209G>A	ENSP00000353178.4:n.725+209G>A
ENST00000597312.5:n.1253+209G>A
ENST00000597921.5:c.728+209G>A	ENSP00000471974.1:n.728+209G>A
ENST00000597934.1:n.1090+209G>A
ENST00000598803.5:n.1223+209G>A
NM_001207019.2:c.725+209G>A	NP_001193948.2:n.725+209G>A
NM_001220500.1:c.728+209G>A	NP_001207429.1:n.728+209G>A
NM_002002.4:c.728+209G>A	NP_001993.2:n.728+209G>A
XM_005272462.3:c.728+209G>A	XP_005272519.1:n.728+209G>A
XM_005272462.4:c.728+209G>A	XP_005272519.1:n.728+209G>A
NM_001220500.2:c.728+209G>A MANE Select	NP_001207429.1:n.728+209G>A
NM_001207019.3:c.725+209G>A	NP_001193948.2:n.725+209G>A
NM_002002.5:c.728+209G>A	NP_001993.2:n.728+209G>A