Canonical Allele Identifier: CA385810498
Gene: BBS10 HGNC NCBI

Linked Data

gnomAD v4: 12-76346292-T-G
MyVariant Identifiers: chr12:g.76740072T>G (hg19) chr12:g.76346292T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346292T>G , CM000674.2:g.76346292T>G GRCh38
NC_000012.11:g.76740072T>G , CM000674.1:g.76740072T>G GRCh37
NC_000012.10:g.75264203T>G NCBI36
NG_016357.1:g.7151A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1693A>C MANE Select ENSP00000497413.1:p.Thr565Pro
ENST00000393262.3:c.1693A>C ENSP00000376946.3:p.Thr565Pro
NM_024685.3:c.1693A>C NP_078961.3:p.Thr565Pro
NM_024685.4:c.1693A>C MANE Select NP_078961.3:p.Thr565Pro
Search 100 bp 5'
Search 100 bp 3'