Canonical Allele Identifier: CA385810489
Gene: BBS10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.76740069T>A (hg19) chr12:g.76346289T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346289T>A , CM000674.2:g.76346289T>A GRCh38
NC_000012.11:g.76740069T>A , CM000674.1:g.76740069T>A GRCh37
NC_000012.10:g.75264200T>A NCBI36
NG_016357.1:g.7154A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1696A>T MANE Select ENSP00000497413.1:p.Asn566Tyr
ENST00000393262.3:c.1696A>T ENSP00000376946.3:p.Asn566Tyr
NM_024685.3:c.1696A>T NP_078961.3:p.Asn566Tyr
NM_024685.4:c.1696A>T MANE Select NP_078961.3:p.Asn566Tyr
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Search 100 bp 3'