Canonical Allele Identifier: CA276773616
Gene: GFER HGNC NCBI

Linked Data

dbSNP Id: rs1046494
MyVariant Identifiers: chr16:g.2036044G>A (hg19) chr16:g.1986043G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1986043G>A , CM000678.2:g.1986043G>A GRCh38
NC_000016.9:g.2036044G>A , CM000678.1:g.2036044G>A GRCh37
NC_000016.8:g.1976045G>A NCBI36
NG_016288.1:g.6895G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.*15G>A ENSP00000455885.1:n.*15G>A
ENST00000248114.7:c.*15G>A MANE Select ENSP00000248114.6:n.*15G>A
ENST00000248114.6:c.*15G>A ENSP00000248114.6:n.*15G>A
ENST00000565658.1:n.790G>A
ENST00000567719.1:c.*15G>A ENSP00000455885.1:n.*15G>A
ENST00000569451.1:c.*106G>A ENSP00000456432.1:n.*106G>A
NM_005262.2:c.*15G>A NP_005253.3:n.*15G>A
NM_005262.3:c.*15G>A MANE Select NP_005253.3:n.*15G>A
Search 100 bp 5'
Search 100 bp 3'