Canonical Allele Identifier: CA2580583865
Gene: GBP6 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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