Canonical Allele Identifier: CA824446613

Gene: BTBD9

Linked Data

• dbSNP Id: rs1433770679
• MyVariant Identifiers: chr6:g.38365887C>T (hg19) ; chr6:g.38398111C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38398111C>T , CM000668.2:g.38398111C>T	GRCh38
NC_000006.11:g.38365887C>T , CM000668.1:g.38365887C>T	GRCh37
NC_000006.10:g.38473865C>T	NCBI36
NG_016545.1:g.247038G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000481247.6:c.1155-53018G>A MANE Select	ENSP00000418751.1:n.1155-53018G>A
ENST00000649492.1:c.1155-53018G>A	ENSP00000497066.1:n.1155-53018G>A
ENST00000314100.10:c.951-53018G>A	ENSP00000323408.6:n.951-53018G>A
ENST00000328403.10:c.*63-53018G>A	ENSP00000328328.6:n.*63-53018G>A
ENST00000419706.6:c.1064+4706G>A	ENSP00000415365.2:n.1064+4706G>A
ENST00000481247.5:c.1155-53018G>A	ENSP00000418751.1:n.1155-53018G>A
NM_001099272.1:c.1155-53018G>A	NP_001092742.1:n.1155-53018G>A
NM_001172418.1:c.1064+4706G>A	NP_001165889.1:n.1064+4706G>A
NM_052893.1:c.1155-53018G>A	NP_443125.1:n.1155-53018G>A
NM_152733.2:c.951-53018G>A	NP_689946.2:n.951-53018G>A
XM_005248841.2:c.1155-53018G>A	XP_005248898.1:n.1155-53018G>A
XM_011514279.1:c.1155-53018G>A	XP_011512581.1:n.1155-53018G>A
XM_011514281.1:c.1155-52841G>A	XP_011512583.1:n.1155-52841G>A
XM_011514279.3:c.1155-53018G>A	XP_011512581.1:n.1155-53018G>A
XM_011514281.3:c.1155-52841G>A	XP_011512583.1:n.1155-52841G>A
NM_001099272.2:c.1155-53018G>A MANE Select	NP_001092742.1:n.1155-53018G>A
NM_052893.2:c.1155-53018G>A	NP_443125.1:n.1155-53018G>A
NM_001172418.2:c.1064+4706G>A	NP_001165889.1:n.1064+4706G>A
NM_152733.3:c.951-53018G>A	NP_689946.2:n.951-53018G>A