Canonical Allele Identifier: CA403106951

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755098G>C (hg19) ; chr19:g.7690212G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690212G>C , CM000681.2:g.7690212G>C	GRCh38
NC_000019.9:g.7755098G>C , CM000681.1:g.7755098G>C	GRCh37
NC_000019.8:g.7661098G>C	NCBI36
NG_029554.1:g.16935C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.675C>G MANE Select	ENSP00000471974.1:p.Asn225Lys
ENST00000346664.9:c.675C>G	ENSP00000264072.6:p.Asn225Lys
ENST00000360067.8:c.672C>G	ENSP00000353178.4:p.Asn224Lys
ENST00000597312.5:n.1200C>G
ENST00000597921.5:c.675C>G	ENSP00000471974.1:p.Asn225Lys
ENST00000597934.1:n.1037C>G
ENST00000598803.5:n.1170C>G
NM_001207019.2:c.672C>G	NP_001193948.2:p.Asn224Lys
NM_001220500.1:c.675C>G	NP_001207429.1:p.Asn225Lys
NM_002002.4:c.675C>G	NP_001993.2:p.Asn225Lys
XM_005272462.3:c.675C>G	XP_005272519.1:p.Asn225Lys
XM_005272462.4:c.675C>G	XP_005272519.1:p.Asn225Lys
NM_001220500.2:c.675C>G MANE Select	NP_001207429.1:p.Asn225Lys
NM_001207019.3:c.672C>G	NP_001193948.2:p.Asn224Lys
NM_002002.5:c.675C>G	NP_001993.2:p.Asn225Lys