Canonical Allele Identifier: CA403108970

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755371G>C (hg19) ; chr19:g.7690485G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690485G>C , CM000681.2:g.7690485G>C	GRCh38
NC_000019.9:g.7755371G>C , CM000681.1:g.7755371G>C	GRCh37
NC_000019.8:g.7661371G>C	NCBI36
NG_029554.1:g.16662C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.542C>G MANE Select	ENSP00000471974.1:p.Thr181Ser
ENST00000346664.9:c.542C>G	ENSP00000264072.6:p.Thr181Ser
ENST00000360067.8:c.539C>G	ENSP00000353178.4:p.Thr180Ser
ENST00000597312.5:n.1067C>G
ENST00000597921.5:c.542C>G	ENSP00000471974.1:p.Thr181Ser
ENST00000597934.1:n.904C>G
ENST00000598803.5:n.1037C>G
NM_001207019.2:c.539C>G	NP_001193948.2:p.Thr180Ser
NM_001220500.1:c.542C>G	NP_001207429.1:p.Thr181Ser
NM_002002.4:c.542C>G	NP_001993.2:p.Thr181Ser
XM_005272462.3:c.542C>G	XP_005272519.1:p.Thr181Ser
XM_005272462.4:c.542C>G	XP_005272519.1:p.Thr181Ser
NM_001220500.2:c.542C>G MANE Select	NP_001207429.1:p.Thr181Ser
NM_001207019.3:c.539C>G	NP_001193948.2:p.Thr180Ser
NM_002002.5:c.542C>G	NP_001993.2:p.Thr181Ser