Canonical Allele Identifier: CA631318386

Gene: FCER2

Linked Data

• dbSNP Id: rs1568486713
• gnomAD v2: 19-7755485-GCCTTGGGCA-G
• gnomAD v4: 19-7690599-GCCTTGGGCA-G
• MyVariant Identifiers: chr19:g.7755486_7755494del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690602_7690610del , CM000681.2:g.7690602_7690610del	GRCh38
NC_000019.9:g.7755488_7755496del , CM000681.1:g.7755488_7755496del	GRCh37
NC_000019.8:g.7661488_7661496del	NCBI36
NG_029554.1:g.16539_16547del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-51_470-43del MANE Select	ENSP00000471974.1:n.470-51_470-43del
ENST00000346664.9:c.470-51_470-43del	ENSP00000264072.6:n.470-51_470-43del
ENST00000360067.8:c.467-51_467-43del	ENSP00000353178.4:n.467-51_467-43del
ENST00000593418.1:c.407-51_407-43del	ENSP00000472067.1:n.407-51_407-43del
ENST00000597312.5:n.995-51_995-43del
ENST00000597921.5:c.470-51_470-43del	ENSP00000471974.1:n.470-51_470-43del
ENST00000597934.1:n.832-51_832-43del
ENST00000598803.5:n.965-51_965-43del
NM_001207019.2:c.467-51_467-43del	NP_001193948.2:n.467-51_467-43del
NM_001220500.1:c.470-51_470-43del	NP_001207429.1:n.470-51_470-43del
NM_002002.4:c.470-51_470-43del	NP_001993.2:n.470-51_470-43del
XM_005272462.3:c.470-51_470-43del	XP_005272519.1:n.470-51_470-43del
XM_005272462.4:c.470-51_470-43del	XP_005272519.1:n.470-51_470-43del
NM_001220500.2:c.470-51_470-43del MANE Select	NP_001207429.1:n.470-51_470-43del
NM_001207019.3:c.467-51_467-43del	NP_001193948.2:n.467-51_467-43del
NM_002002.5:c.470-51_470-43del	NP_001993.2:n.470-51_470-43del