Canonical Allele Identifier: CA492950304
Gene: GFER HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2036005C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1986004C>T , CM000678.2:g.1986004C>T GRCh38
NC_000016.9:g.2036005C>T , CM000678.1:g.2036005C>T GRCh37
NC_000016.8:g.1976006C>T NCBI36
NG_016288.1:g.6856C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.369C>T ENSP00000455885.1:p.Gly123=
ENST00000248114.7:c.594C>T MANE Select ENSP00000248114.6:p.Gly198=
ENST00000248114.6:c.594C>T ENSP00000248114.6:p.Gly198=
ENST00000565658.1:n.751C>T
ENST00000567719.1:c.369C>T ENSP00000455885.1:p.Gly123=
ENST00000569451.1:c.*67C>T ENSP00000456432.1:n.*67C>T
NM_005262.2:c.594C>T NP_005253.3:p.Gly198=
NM_005262.3:c.594C>T MANE Select NP_005253.3:p.Gly198=