Canonical Allele Identifier: CA2277279
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 370921
ClinVar RCV Id: RCV000409760
dbSNP Id: rs373249212
gnomAD v2: 3-15677196-G-T
gnomAD v3: 3-15635689-G-T
gnomAD v4: 3-15635689-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15635689G>T , CM000665.2:g.15635689G>T GRCh38
NC_000003.11:g.15677196G>T , CM000665.1:g.15677196G>T GRCh37
NC_000003.10:g.15652200G>T NCBI36
NG_008019.1:g.38942G>T
NG_008019.2:g.39338G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000436193.6:c.249+1G>T ENSP00000394277.2:n.249+1G>T
ENST00000671928.2:c.249+1G>T ENSP00000500069.2:n.249+1G>T
ENST00000672892.2:c.249+1G>T ENSP00000499944.2:n.249+1G>T
ENST00000303498.10:c.249+1G>T ENSP00000306477.6:n.249+1G>T
ENST00000417015.3:c.249+1G>T ENSP00000403775.3:n.249+1G>T
ENST00000427382.2:c.249+1G>T ENSP00000397113.2:n.249+1G>T
ENST00000437172.6:c.249+1G>T ENSP00000400995.2:n.249+1G>T
ENST00000449107.7:c.249+1G>T ENSP00000388212.2:n.249+1G>T
ENST00000467027.6:n.1088+1G>T
ENST00000482824.2:c.249+1G>T ENSP00000494864.1:n.249+1G>T
ENST00000643237.3:c.249+1G>T MANE Select ENSP00000495254.2:n.249+1G>T
ENST00000646371.1:c.249+1G>T ENSP00000495866.1:n.249+1G>T
ENST00000671928.1:c.15+1G>T ENSP00000500069.1:n.15+1G>T
ENST00000672065.1:c.309+1G>T ENSP00000500403.1:n.309+1G>T
ENST00000672112.1:c.315+1G>T ENSP00000500193.1:n.315+1G>T
ENST00000672141.1:c.249+1G>T ENSP00000500210.1:n.249+1G>T
ENST00000672336.1:c.249+1G>T ENSP00000500267.1:n.249+1G>T
ENST00000672427.1:c.249+1G>T ENSP00000500131.1:n.249+1G>T
ENST00000672760.1:c.249+1G>T ENSP00000500530.1:n.249+1G>T
ENST00000672892.1:c.27+1G>T ENSP00000499944.1:n.27+1G>T
ENST00000673467.1:c.249+1G>T ENSP00000500288.1:n.249+1G>T
ENST00000673620.1:c.249+1G>T ENSP00000500325.1:n.249+1G>T
ENST00000303498.9:c.309+1G>T ENSP00000306477.5:n.309+1G>T
ENST00000383778.5:c.249+1G>T ENSP00000373288.4:n.249+1G>T
ENST00000436193.5:c.249+1G>T ENSP00000394277.1:n.249+1G>T
ENST00000437172.5:c.315+1G>T ENSP00000400995.1:n.315+1G>T
ENST00000449107.5:c.315+1G>T ENSP00000388212.1:n.315+1G>T
ENST00000482824.1:n.384+1G>T
NM_000060.3:c.309+1G>T NP_000051.1:n.309+1G>T
NM_001281723.1:c.315+1G>T NP_001268652.1:n.315+1G>T
NM_001281724.1:c.315+1G>T NP_001268653.1:n.315+1G>T
NM_001281725.1:c.249+1G>T NP_001268654.1:n.249+1G>T
NM_001281726.1:c.309+1G>T NP_001268655.1:n.309+1G>T
XM_006713314.2:c.249+1G>T XP_006713377.1:n.249+1G>T
XM_011534041.1:c.249+1G>T XP_011532343.1:n.249+1G>T
NM_000060.4:c.309+1G>T NP_000051.1:n.309+1G>T
NM_001281723.2:c.315+1G>T NP_001268652.1:n.315+1G>T
NM_001281724.2:c.315+1G>T NP_001268653.1:n.315+1G>T
NM_001281725.2:c.249+1G>T NP_001268654.1:n.249+1G>T
NM_001323582.1:c.249+1G>T NP_001310511.1:n.249+1G>T
XM_011534041.2:c.249+1G>T XP_011532343.1:n.249+1G>T
XM_017007088.1:c.249+1G>T XP_016862577.1:n.249+1G>T
XM_024453724.1:c.249+1G>T XP_024309492.1:n.249+1G>T
NM_001281723.3:c.249+1G>T NP_001268652.2:n.249+1G>T
NM_001281724.3:c.249+1G>T NP_001268653.2:n.249+1G>T
NM_001370658.1:c.249+1G>T MANE Select NP_001357587.1:n.249+1G>T
NM_001370752.1:c.249+1G>T NP_001357681.1:n.249+1G>T
NM_001370753.1:c.249+1G>T NP_001357682.1:n.249+1G>T
NM_001281726.2:c.249+1G>T NP_001268655.2:n.249+1G>T