Canonical Allele Identifier: CA884237729

Gene: FCER2

Linked Data

• dbSNP Id: rs149647877
• gnomAD v3: 19-7690348-G-C
• gnomAD v4: 19-7690348-G-C
• MyVariant Identifiers: chr19:g.7755234G>C (hg19) ; chr19:g.7690348G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690348G>C , CM000681.2:g.7690348G>C	GRCh38
NC_000019.9:g.7755234G>C , CM000681.1:g.7755234G>C	GRCh37
NC_000019.8:g.7661234G>C	NCBI36
NG_029554.1:g.16799C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.621+58C>G MANE Select	ENSP00000471974.1:n.621+58C>G
ENST00000346664.9:c.621+58C>G	ENSP00000264072.6:n.621+58C>G
ENST00000360067.8:c.618+58C>G	ENSP00000353178.4:n.618+58C>G
ENST00000597312.5:n.1146+58C>G
ENST00000597921.5:c.621+58C>G	ENSP00000471974.1:n.621+58C>G
ENST00000597934.1:n.983+58C>G
ENST00000598803.5:n.1116+58C>G
NM_001207019.2:c.618+58C>G	NP_001193948.2:n.618+58C>G
NM_001220500.1:c.621+58C>G	NP_001207429.1:n.621+58C>G
NM_002002.4:c.621+58C>G	NP_001993.2:n.621+58C>G
XM_005272462.3:c.621+58C>G	XP_005272519.1:n.621+58C>G
XM_005272462.4:c.621+58C>G	XP_005272519.1:n.621+58C>G
NM_001220500.2:c.621+58C>G MANE Select	NP_001207429.1:n.621+58C>G
NM_001207019.3:c.618+58C>G	NP_001193948.2:n.618+58C>G
NM_002002.5:c.621+58C>G	NP_001993.2:n.621+58C>G