Canonical Allele Identifier: CA129721
Gene: GLCCI1-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.8007876G>G (hg19) chr7:g.7968245G>G (hg38)
PubMed: PMID:21991891
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.7968245G= , CM000669.2:g.7968245G= GRCh38
NC_000007.13:g.8007876G= , CM000669.1:g.8007876G= GRCh37
NC_000007.12:g.7974401G= NCBI36
NG_032073.1:g.4503G=

Transcript Alleles

HGVS Amino-acid Change
NR_110018.1:n.209+299C=
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