Canonical Allele Identifier: CA403107333

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755124T>G (hg19) ; chr19:g.7690238T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690238T>G , CM000681.2:g.7690238T>G	GRCh38
NC_000019.9:g.7755124T>G , CM000681.1:g.7755124T>G	GRCh37
NC_000019.8:g.7661124T>G	NCBI36
NG_029554.1:g.16909A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.649A>C MANE Select	ENSP00000471974.1:p.Thr217Pro
ENST00000346664.9:c.649A>C	ENSP00000264072.6:p.Thr217Pro
ENST00000360067.8:c.646A>C	ENSP00000353178.4:p.Thr216Pro
ENST00000597312.5:n.1174A>C
ENST00000597921.5:c.649A>C	ENSP00000471974.1:p.Thr217Pro
ENST00000597934.1:n.1011A>C
ENST00000598803.5:n.1144A>C
NM_001207019.2:c.646A>C	NP_001193948.2:p.Thr216Pro
NM_001220500.1:c.649A>C	NP_001207429.1:p.Thr217Pro
NM_002002.4:c.649A>C	NP_001993.2:p.Thr217Pro
XM_005272462.3:c.649A>C	XP_005272519.1:p.Thr217Pro
XM_005272462.4:c.649A>C	XP_005272519.1:p.Thr217Pro
NM_001220500.2:c.649A>C MANE Select	NP_001207429.1:p.Thr217Pro
NM_001207019.3:c.646A>C	NP_001193948.2:p.Thr216Pro
NM_002002.5:c.649A>C	NP_001993.2:p.Thr217Pro