Canonical Allele Identifier: CA631318376

Gene: FCER2

Linked Data

• dbSNP Id: rs1432377890
• gnomAD v2: 19-7755477-ATG-A
• MyVariant Identifiers: chr19:g.7755478_7755479del (hg19) ; chr19:g.7690592_7690593del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690592_7690593del , CM000681.2:g.7690592_7690593del	GRCh38
NC_000019.9:g.7755478_7755479del , CM000681.1:g.7755478_7755479del	GRCh37
NC_000019.8:g.7661478_7661479del	NCBI36
NG_029554.1:g.16554_16555del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-36_470-35del MANE Select	ENSP00000471974.1:n.470-36_470-35del
ENST00000346664.9:c.470-36_470-35del	ENSP00000264072.6:n.470-36_470-35del
ENST00000360067.8:c.467-36_467-35del	ENSP00000353178.4:n.467-36_467-35del
ENST00000593418.1:c.407-36_407-35del	ENSP00000472067.1:n.407-36_407-35del
ENST00000597312.5:n.995-36_995-35del
ENST00000597921.5:c.470-36_470-35del	ENSP00000471974.1:n.470-36_470-35del
ENST00000597934.1:n.832-36_832-35del
ENST00000598803.5:n.965-36_965-35del
NM_001207019.2:c.467-36_467-35del	NP_001193948.2:n.467-36_467-35del
NM_001220500.1:c.470-36_470-35del	NP_001207429.1:n.470-36_470-35del
NM_002002.4:c.470-36_470-35del	NP_001993.2:n.470-36_470-35del
XM_005272462.3:c.470-36_470-35del	XP_005272519.1:n.470-36_470-35del
XM_005272462.4:c.470-36_470-35del	XP_005272519.1:n.470-36_470-35del
NM_001220500.2:c.470-36_470-35del MANE Select	NP_001207429.1:n.470-36_470-35del
NM_001207019.3:c.467-36_467-35del	NP_001193948.2:n.467-36_467-35del
NM_002002.5:c.470-36_470-35del	NP_001993.2:n.470-36_470-35del