Canonical Allele Identifier: CA505404854

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755101C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690215C>G , CM000681.2:g.7690215C>G	GRCh38
NC_000019.9:g.7755101C>G , CM000681.1:g.7755101C>G	GRCh37
NC_000019.8:g.7661101C>G	NCBI36
NG_029554.1:g.16932G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.672G>C MANE Select	ENSP00000471974.1:p.Arg224=
ENST00000346664.9:c.672G>C	ENSP00000264072.6:p.Arg224=
ENST00000360067.8:c.669G>C	ENSP00000353178.4:p.Arg223=
ENST00000597312.5:n.1197G>C
ENST00000597921.5:c.672G>C	ENSP00000471974.1:p.Arg224=
ENST00000597934.1:n.1034G>C
ENST00000598803.5:n.1167G>C
NM_001207019.2:c.669G>C	NP_001193948.2:p.Arg223=
NM_001220500.1:c.672G>C	NP_001207429.1:p.Arg224=
NM_002002.4:c.672G>C	NP_001993.2:p.Arg224=
XM_005272462.3:c.672G>C	XP_005272519.1:p.Arg224=
XM_005272462.4:c.672G>C	XP_005272519.1:p.Arg224=
NM_001220500.2:c.672G>C MANE Select	NP_001207429.1:p.Arg224=
NM_001207019.3:c.669G>C	NP_001193948.2:p.Arg223=
NM_002002.5:c.672G>C	NP_001993.2:p.Arg224=