Canonical Allele Identifier: CA1139841166

Gene: GBP6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.89384015G= , CM000663.2:g.89384015G=	GRCh38
NC_000001.10:g.89849574G= , CM000663.1:g.89849574G=	GRCh37
NC_000001.9:g.89622162G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370456.5:c.1469-78G= MANE Select	ENSP00000359485.5:n.1469-78G=
ENST00000370456.4:c.1469-78G=	ENSP00000359485.4:n.1469-78G=
NM_198460.2:c.1469-78G=	NP_940862.2:n.1469-78G=
XM_005270549.3:c.1079-78G=	XP_005270606.1:n.1079-78G=
XM_011540835.1:c.1469-78G=	XP_011539137.1:n.1469-78G=
NM_001320257.1:c.1079-78G=	NP_001307186.1:n.1079-78G=
XM_011540835.3:c.1469-78G=	XP_011539137.1:n.1469-78G=
NM_198460.3:c.1469-78G= MANE Select	NP_940862.2:n.1469-78G=
NM_001320257.2:c.1079-78G=	NP_001307186.1:n.1079-78G=