Canonical Allele Identifier: CA403106409

Gene: FCER2

Linked Data

• dbSNP Id: rs1599431333
• MyVariant Identifiers: chr19:g.7755058G>A (hg19) ; chr19:g.7690172G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690172G>A , CM000681.2:g.7690172G>A	GRCh38
NC_000019.9:g.7755058G>A , CM000681.1:g.7755058G>A	GRCh37
NC_000019.8:g.7661058G>A	NCBI36
NG_029554.1:g.16975C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.715C>T MANE Select	ENSP00000471974.1:p.His239Tyr
ENST00000346664.9:c.715C>T	ENSP00000264072.6:p.His239Tyr
ENST00000360067.8:c.712C>T	ENSP00000353178.4:p.His238Tyr
ENST00000597312.5:n.1240C>T
ENST00000597921.5:c.715C>T	ENSP00000471974.1:p.His239Tyr
ENST00000597934.1:n.1077C>T
ENST00000598803.5:n.1210C>T
NM_001207019.2:c.712C>T	NP_001193948.2:p.His238Tyr
NM_001220500.1:c.715C>T	NP_001207429.1:p.His239Tyr
NM_002002.4:c.715C>T	NP_001993.2:p.His239Tyr
XM_005272462.3:c.715C>T	XP_005272519.1:p.His239Tyr
XM_005272462.4:c.715C>T	XP_005272519.1:p.His239Tyr
NM_001220500.2:c.715C>T MANE Select	NP_001207429.1:p.His239Tyr
NM_001207019.3:c.712C>T	NP_001193948.2:p.His238Tyr
NM_002002.5:c.715C>T	NP_001993.2:p.His239Tyr