Canonical Allele Identifier: CA631318371

Gene: FCER2

Linked Data

• gnomAD v2: 19-7755469-TGGG-T
• gnomAD v4: 19-7690583-TGGG-T
• MyVariant Identifiers: chr19:g.7755470_7755472del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690585_7690587del , CM000681.2:g.7690585_7690587del	GRCh38
NC_000019.9:g.7755471_7755473del , CM000681.1:g.7755471_7755473del	GRCh37
NC_000019.8:g.7661471_7661473del	NCBI36
NG_029554.1:g.16561_16563del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-29_470-27del MANE Select	ENSP00000471974.1:n.470-29_470-27del
ENST00000346664.9:c.470-29_470-27del	ENSP00000264072.6:n.470-29_470-27del
ENST00000360067.8:c.467-29_467-27del	ENSP00000353178.4:n.467-29_467-27del
ENST00000593418.1:c.407-29_407-27del	ENSP00000472067.1:n.407-29_407-27del
ENST00000597312.5:n.995-29_995-27del
ENST00000597921.5:c.470-29_470-27del	ENSP00000471974.1:n.470-29_470-27del
ENST00000597934.1:n.832-29_832-27del
ENST00000598803.5:n.965-29_965-27del
NM_001207019.2:c.467-29_467-27del	NP_001193948.2:n.467-29_467-27del
NM_001220500.1:c.470-29_470-27del	NP_001207429.1:n.470-29_470-27del
NM_002002.4:c.470-29_470-27del	NP_001993.2:n.470-29_470-27del
XM_005272462.3:c.470-29_470-27del	XP_005272519.1:n.470-29_470-27del
XM_005272462.4:c.470-29_470-27del	XP_005272519.1:n.470-29_470-27del
NM_001220500.2:c.470-29_470-27del MANE Select	NP_001207429.1:n.470-29_470-27del
NM_001207019.3:c.467-29_467-27del	NP_001193948.2:n.467-29_467-27del
NM_002002.5:c.470-29_470-27del	NP_001993.2:n.470-29_470-27del