Canonical Allele Identifier: CA239331437
Gene: BBS10 HGNC NCBI

Linked Data

dbSNP Id: rs915187837
MyVariant Identifiers: chr12:g.76739698A>T (hg19) chr12:g.76345918A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76345918A>T , CM000674.2:g.76345918A>T GRCh38
NC_000012.11:g.76739698A>T , CM000674.1:g.76739698A>T GRCh37
NC_000012.10:g.75263829A>T NCBI36
NG_016357.1:g.7525T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.2067T>A MANE Select ENSP00000497413.1:p.Thr689=
ENST00000393262.3:c.2067T>A ENSP00000376946.3:p.Thr689=
NM_024685.3:c.2067T>A NP_078961.3:p.Thr689=
NM_024685.4:c.2067T>A MANE Select NP_078961.3:p.Thr689=
Search 100 bp 5'
Search 100 bp 3'