Canonical Allele Identifier: CA718840228
Gene: GFER HGNC NCBI

Linked Data

dbSNP Id: rs1204175194
MyVariant Identifiers: chr16:g.2036054G>A (hg19) chr16:g.1986053G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1986053G>A , CM000678.2:g.1986053G>A GRCh38
NC_000016.9:g.2036054G>A , CM000678.1:g.2036054G>A GRCh37
NC_000016.8:g.1976055G>A NCBI36
NG_016288.1:g.6905G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.*25G>A ENSP00000455885.1:n.*25G>A
ENST00000248114.7:c.*25G>A MANE Select ENSP00000248114.6:n.*25G>A
ENST00000248114.6:c.*25G>A ENSP00000248114.6:n.*25G>A
ENST00000565658.1:n.800G>A
ENST00000567719.1:c.*25G>A ENSP00000455885.1:n.*25G>A
ENST00000569451.1:c.*116G>A ENSP00000456432.1:n.*116G>A
NM_005262.2:c.*25G>A NP_005253.3:n.*25G>A
NM_005262.3:c.*25G>A MANE Select NP_005253.3:n.*25G>A
Search 100 bp 5'
Search 100 bp 3'