Canonical Allele Identifier: CA691951486
Gene: BBS10 HGNC NCBI

Linked Data

dbSNP Id: rs1252053696
gnomAD v3: 12-76345771-T-A
gnomAD v4: 12-76345771-T-A
MyVariant Identifiers: chr12:g.76739551T>A (hg19) chr12:g.76345771T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76345771T>A , CM000674.2:g.76345771T>A GRCh38
NC_000012.11:g.76739551T>A , CM000674.1:g.76739551T>A GRCh37
NC_000012.10:g.75263682T>A NCBI36
NG_016357.1:g.7672A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.*42A>T MANE Select ENSP00000497413.1:n.*42A>T
ENST00000393262.3:c.*42A>T ENSP00000376946.3:n.*42A>T
NM_024685.3:c.*42A>T NP_078961.3:n.*42A>T
NM_024685.4:c.*42A>T MANE Select NP_078961.3:n.*42A>T
Search 100 bp 5'
Search 100 bp 3'