Canonical Allele Identifier: CA394303696
Gene: GFER HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2035876G>C (hg19) chr16:g.1985875G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985875G>C , CM000678.2:g.1985875G>C GRCh38
NC_000016.9:g.2035876G>C , CM000678.1:g.2035876G>C GRCh37
NC_000016.8:g.1975877G>C NCBI36
NG_016288.1:g.6727G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.240G>C ENSP00000455885.1:p.Arg80Ser
ENST00000248114.7:c.465G>C MANE Select ENSP00000248114.6:p.Arg155Ser
ENST00000248114.6:c.465G>C ENSP00000248114.6:p.Arg155Ser
ENST00000565658.1:n.622G>C
ENST00000567719.1:c.240G>C ENSP00000455885.1:p.Arg80Ser
ENST00000569451.1:c.268G>C ENSP00000456432.1:p.Glu90Gln
NM_005262.2:c.465G>C NP_005253.3:p.Arg155Ser
NM_005262.3:c.465G>C MANE Select NP_005253.3:p.Arg155Ser
Search 100 bp 5'
Search 100 bp 3'