Canonical Allele Identifier: CA403108343
Gene: FCER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7690437T>G , CM000681.2:g.7690437T>G GRCh38
NC_000019.9:g.7755323T>G , CM000681.1:g.7755323T>G GRCh37
NC_000019.8:g.7661323T>G NCBI36
NG_029554.1:g.16710A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000597921.6:c.590A>C MANE Select ENSP00000471974.1:p.Gln197Pro
ENST00000346664.9:c.590A>C ENSP00000264072.6:p.Gln197Pro
ENST00000360067.8:c.587A>C ENSP00000353178.4:p.Gln196Pro
ENST00000597312.5:n.1115A>C
ENST00000597921.5:c.590A>C ENSP00000471974.1:p.Gln197Pro
ENST00000597934.1:n.952A>C
ENST00000598803.5:n.1085A>C
NM_001207019.2:c.587A>C NP_001193948.2:p.Gln196Pro
NM_001220500.1:c.590A>C NP_001207429.1:p.Gln197Pro
NM_002002.4:c.590A>C NP_001993.2:p.Gln197Pro
XM_005272462.3:c.590A>C XP_005272519.1:p.Gln197Pro
XM_005272462.4:c.590A>C XP_005272519.1:p.Gln197Pro
NM_001220500.2:c.590A>C MANE Select NP_001207429.1:p.Gln197Pro
NM_001207019.3:c.587A>C NP_001193948.2:p.Gln196Pro
NM_002002.5:c.590A>C NP_001993.2:p.Gln197Pro