Canonical Allele Identifier: CA428559505
Gene: GLI2 HGNC NCBI

Linked Data

dbSNP Id: rs1397595368

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990657C>T , CM000664.2:g.120990657C>T GRCh38
NC_000002.11:g.121748233C>T , CM000664.1:g.121748233C>T GRCh37
NC_000002.10:g.121464703C>T NCBI36
NG_009030.1:g.198367C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4692C>T MANE Select ENSP00000354586.5:p.Phe1564=
ENST00000452319.6:c.4743C>T ENSP00000390436.1:p.Phe1581=
ENST00000341310.10:c.*3791C>T ENSP00000344473.6:n.*3791C>T
ENST00000361492.8:c.4743C>T ENSP00000354586.4:p.Phe1581=
ENST00000438299.5:c.*2611C>T ENSP00000400593.1:n.*2611C>T
ENST00000445186.5:c.*3842C>T ENSP00000397488.1:n.*3842C>T
ENST00000452319.5:c.4743C>T ENSP00000390436.1:p.Phe1581=
ENST00000452692.5:c.*2560C>T ENSP00000403715.1:n.*2560C>T
NM_005270.4:c.4743C>T NP_005261.2:p.Phe1581=
XM_006712422.1:c.4692C>T XP_006712485.1:p.Phe1564=
XM_011510969.1:c.4725C>T XP_011509271.1:p.Phe1575=
XM_011510970.1:c.4602C>T XP_011509272.1:p.Phe1534=
XM_011510971.1:c.4548C>T XP_011509273.1:p.Phe1516=
XM_011510972.1:c.4548C>T XP_011509274.1:p.Phe1516=
XM_011510973.1:c.4368C>T XP_011509275.1:p.Phe1456=
XM_011510974.1:c.4317C>T XP_011509276.1:p.Phe1439=
XM_006712422.3:c.4692C>T XP_006712485.1:p.Phe1564=
XM_011510969.2:c.4995C>T XP_011509271.2:p.Phe1665=
XM_011510970.2:c.4602C>T XP_011509272.1:p.Phe1534=
XM_011510971.2:c.4548C>T XP_011509273.1:p.Phe1516=
XM_011510972.2:c.4644C>T XP_011509274.2:p.Phe1548=
XM_011510973.2:c.4368C>T XP_011509275.1:p.Phe1456=
XM_011510974.2:c.4317C>T XP_011509276.1:p.Phe1439=
XM_017003818.1:c.4944C>T XP_016859307.1:p.Phe1648=
XM_024452794.1:c.4743C>T XP_024308562.1:p.Phe1581=
XM_024452795.1:c.4743C>T XP_024308563.1:p.Phe1581=
NM_001371271.1:c.4743C>T NP_001358200.1:p.Phe1581=
NM_001374353.1:c.4692C>T MANE Select NP_001361282.1:p.Phe1564=
NM_001374354.1:c.4317C>T NP_001361283.1:p.Phe1439=
NM_005270.5:c.4743C>T NP_005261.2:p.Phe1581=