Canonical Allele Identifier: CA367321628
Gene: GLI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.42007446C>G (hg19) chr7:g.41967848C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41967848C>G , CM000669.2:g.41967848C>G GRCh38
NC_000007.13:g.42007446C>G , CM000669.1:g.42007446C>G GRCh37
NC_000007.12:g.41973971C>G NCBI36
NG_008434.1:g.274173G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.2179G>C MANE Select ENSP00000379258.3:p.Gly727Arg
ENST00000677288.1:c.2005G>C ENSP00000503986.1:p.Gly669Arg
ENST00000677605.1:c.2179G>C ENSP00000503743.1:p.Gly727Arg
ENST00000678429.1:c.2179G>C ENSP00000502957.1:p.Gly727Arg
ENST00000395925.7:c.2179G>C ENSP00000379258.3:p.Gly727Arg
ENST00000479210.1:n.2156G>C
NM_000168.5:c.2179G>C NP_000159.3:p.Gly727Arg
XM_005249703.1:c.2179G>C XP_005249760.1:p.Gly727Arg
XM_005249704.2:c.2179G>C XP_005249761.1:p.Gly727Arg
XM_011515272.1:c.2179G>C XP_011513574.1:p.Gly727Arg
XM_011515273.1:c.2179G>C XP_011513575.1:p.Gly727Arg
XM_011515274.1:c.2002G>C XP_011513576.1:p.Gly668Arg
XM_011515274.2:c.2002G>C XP_011513576.1:p.Gly668Arg
XM_017011997.1:c.2176G>C XP_016867486.1:p.Gly726Arg
NM_000168.6:c.2179G>C MANE Select NP_000159.3:p.Gly727Arg
Search 100 bp 5'
Search 100 bp 3'