Canonical Allele Identifier: CA15448665
Gene: BTBD9 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs9357271

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38398097T>C , CM000668.2:g.38398097T>C GRCh38
NC_000006.10:g.38473851T>C NCBI36
NC_000006.11:g.38365873T>C , CM000668.1:g.38365873T>C GRCh37
NG_016545.1:g.247052A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000314100.10:c.951-53004A>G ENSP00000323408.6:p.=
ENST00000328403.10:c.*63-53004A>G ENSP00000328328.6:p.=
ENST00000419706.6:c.1064+4720A>G ENSP00000415365.2:p.=
ENST00000481247.5:c.1155-53004A>G ENSP00000418751.1:p.=
NM_001099272.1:c.1155-53004A>G VV NP_001092742.1:p.=
NM_001172418.1:c.1064+4720A>G VV NP_001165889.1:p.=
NM_052893.1:c.1155-53004A>G VV NP_443125.1:p.=
NM_152733.2:c.951-53004A>G VV NP_689946.2:p.=
XM_005248841.2:c.1155-53004A>G XP_005248898.1:p.=
XM_011514279.1:c.1155-53004A>G XP_011512581.1:p.=
XM_011514281.1:c.1155-52827A>G XP_011512583.1:p.=
XM_011514279.3:c.1155-53004A>G
XM_011514281.3:c.1155-52827A>G