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ClinGen Allele Registry
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Canonical Allele Identifier:
CA2263242613
Community Standard Title: NM_006361.6(HOXB13):c.251G= (p.Gly84=)
Gene: HOXB13
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.48728343C= , CM000679.2:g.48728343C=
GRCh38
NC_000017.10:g.46805705C= , CM000679.1:g.46805705C=
GRCh37
NC_000017.9:g.44160704C=
NCBI36
NG_033789.1:g.5407G= , LRG_771:g.5407G=
Transcript Alleles
HGVS
Amino-acid Change
NM_006361.6:c.251G=
MANE Select
NP_006352.2:p.Gly84=
ENST00000290295.8:c.251G=
MANE Select
ENSP00000290295.8:p.Gly84=
NM_006361.5:c.251G= , LRG_771t1:c.251G=
NP_006352.2:p.Gly84=
ENST00000290295.7:c.251G=
ENSP00000290295.7:p.Gly84=
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