Canonical Allele Identifier: CA884238078

Gene: FCER2

Linked Data

• dbSNP Id: rs1293143385
• gnomAD v4: 19-7690625-T-A
• MyVariant Identifiers: chr19:g.7755511T>A (hg19) ; chr19:g.7690625T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690625T>A , CM000681.2:g.7690625T>A	GRCh38
NC_000019.9:g.7755511T>A , CM000681.1:g.7755511T>A	GRCh37
NC_000019.8:g.7661511T>A	NCBI36
NG_029554.1:g.16522A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-68A>T MANE Select	ENSP00000471974.1:n.470-68A>T
ENST00000346664.9:c.470-68A>T	ENSP00000264072.6:n.470-68A>T
ENST00000360067.8:c.467-68A>T	ENSP00000353178.4:n.467-68A>T
ENST00000593418.1:c.407-68A>T	ENSP00000472067.1:n.407-68A>T
ENST00000597312.5:n.995-68A>T
ENST00000597921.5:c.470-68A>T	ENSP00000471974.1:n.470-68A>T
ENST00000597934.1:n.832-68A>T
ENST00000598803.5:n.965-68A>T
NM_001207019.2:c.467-68A>T	NP_001193948.2:n.467-68A>T
NM_001220500.1:c.470-68A>T	NP_001207429.1:n.470-68A>T
NM_002002.4:c.470-68A>T	NP_001993.2:n.470-68A>T
XM_005272462.3:c.470-68A>T	XP_005272519.1:n.470-68A>T
XM_005272462.4:c.470-68A>T	XP_005272519.1:n.470-68A>T
NM_001220500.2:c.470-68A>T MANE Select	NP_001207429.1:n.470-68A>T
NM_001207019.3:c.467-68A>T	NP_001193948.2:n.467-68A>T
NM_002002.5:c.470-68A>T	NP_001993.2:n.470-68A>T