Canonical Allele Identifier: CA2201967956
Gene: GFER HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1986066G= , CM000678.2:g.1986066G= GRCh38
NC_000016.9:g.2036067G= , CM000678.1:g.2036067G= GRCh37
NC_000016.8:g.1976068G= NCBI36
NG_016288.1:g.6918G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.*38G= ENSP00000455885.1:n.*38G=
ENST00000248114.7:c.*38G= MANE Select ENSP00000248114.6:n.*38G=
ENST00000248114.6:c.*38G= ENSP00000248114.6:n.*38G=
ENST00000565658.1:n.813G=
ENST00000567719.1:c.*38G= ENSP00000455885.1:n.*38G=
ENST00000569451.1:c.*129G= ENSP00000456432.1:n.*129G=
NM_005262.2:c.*38G= NP_005253.3:n.*38G=
NM_005262.3:c.*38G= MANE Select NP_005253.3:n.*38G=
Search 100 bp 5'
Search 100 bp 3'