Canonical Allele Identifier: CA9145010

Gene: FCER2

Linked Data

• dbSNP Id: rs774169912
• ExAC: 19:7755358 G / C
• gnomAD v2: 19-7755358-G-C
• MyVariant Identifiers: chr19:g.7755358G>C (hg19) ; chr19:g.7690472G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690472G>C , CM000681.2:g.7690472G>C	GRCh38
NC_000019.9:g.7755358G>C , CM000681.1:g.7755358G>C	GRCh37
NC_000019.8:g.7661358G>C	NCBI36
NG_029554.1:g.16675C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.555C>G MANE Select	ENSP00000471974.1:p.Val185=
ENST00000346664.9:c.555C>G	ENSP00000264072.6:p.Val185=
ENST00000360067.8:c.552C>G	ENSP00000353178.4:p.Val184=
ENST00000597312.5:n.1080C>G
ENST00000597921.5:c.555C>G	ENSP00000471974.1:p.Val185=
ENST00000597934.1:n.917C>G
ENST00000598803.5:n.1050C>G
NM_001207019.2:c.552C>G	NP_001193948.2:p.Val184=
NM_001220500.1:c.555C>G	NP_001207429.1:p.Val185=
NM_002002.4:c.555C>G	NP_001993.2:p.Val185=
XM_005272462.3:c.555C>G	XP_005272519.1:p.Val185=
XM_005272462.4:c.555C>G	XP_005272519.1:p.Val185=
NM_001220500.2:c.555C>G MANE Select	NP_001207429.1:p.Val185=
NM_001207019.3:c.552C>G	NP_001193948.2:p.Val184=
NM_002002.5:c.555C>G	NP_001993.2:p.Val185=