Canonical Allele Identifier: CA342936
Gene: GLI3 HGNC NCBI

Linked Data

dbSNP Id: rs116840763
MyVariant Identifiers: chr7:g.42005872G>C (hg19) chr7:g.41966274G>C (hg38)
PubMed: PMID:20301638
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41966274G>C , CM000669.2:g.41966274G>C GRCh38
NC_000007.13:g.42005872G>C , CM000669.1:g.42005872G>C GRCh37
NC_000007.12:g.41972397G>C NCBI36
NG_008434.1:g.275747C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.2799C>G MANE Select ENSP00000379258.3:p.Tyr933Ter
ENST00000677288.1:c.2625C>G ENSP00000503986.1:p.Tyr875Ter
ENST00000677605.1:c.2799C>G ENSP00000503743.1:p.Tyr933Ter
ENST00000678429.1:c.2799C>G ENSP00000502957.1:p.Tyr933Ter
ENST00000395925.7:c.2799C>G ENSP00000379258.3:p.Tyr933Ter
ENST00000479210.1:n.2776C>G
NM_000168.5:c.2799C>G NP_000159.3:p.Tyr933Ter
XM_005249703.1:c.2799C>G XP_005249760.1:p.Tyr933Ter
XM_005249704.2:c.2799C>G XP_005249761.1:p.Tyr933Ter
XM_011515272.1:c.2799C>G XP_011513574.1:p.Tyr933Ter
XM_011515273.1:c.2799C>G XP_011513575.1:p.Tyr933Ter
XM_011515274.1:c.2622C>G XP_011513576.1:p.Tyr874Ter
XM_011515274.2:c.2622C>G XP_011513576.1:p.Tyr874Ter
XM_017011997.1:c.2796C>G XP_016867486.1:p.Tyr932Ter
NM_000168.6:c.2799C>G MANE Select NP_000159.3:p.Tyr933Ter
Search 100 bp 5'
Search 100 bp 3'