Canonical Allele Identifier: CA481011100
Gene: BBS10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.76739839T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76346059T>C , CM000674.2:g.76346059T>C GRCh38
NC_000012.11:g.76739839T>C , CM000674.1:g.76739839T>C GRCh37
NC_000012.10:g.75263970T>C NCBI36
NG_016357.1:g.7384A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650064.2:c.1926A>G MANE Select ENSP00000497413.1:p.Lys642=
ENST00000393262.3:c.1926A>G ENSP00000376946.3:p.Lys642=
NM_024685.3:c.1926A>G NP_078961.3:p.Lys642=
NM_024685.4:c.1926A>G MANE Select NP_078961.3:p.Lys642=
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