Canonical Allele Identifier: CA385810716
Gene: BBS10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.76740129T>G (hg19) chr12:g.76346349T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346349T>G , CM000674.2:g.76346349T>G GRCh38
NC_000012.11:g.76740129T>G , CM000674.1:g.76740129T>G GRCh37
NC_000012.10:g.75264260T>G NCBI36
NG_016357.1:g.7094A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650064.2:c.1636A>C MANE Select ENSP00000497413.1:p.Thr546Pro
ENST00000393262.3:c.1636A>C ENSP00000376946.3:p.Thr546Pro
NM_024685.3:c.1636A>C NP_078961.3:p.Thr546Pro
NM_024685.4:c.1636A>C MANE Select NP_078961.3:p.Thr546Pro
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