Canonical Allele Identifier: CA337955737

Gene: GABRD

Linked Data

• ClinVar Variation Id: 3097833
• ClinVar RCV Id: RCV004390146
• dbSNP Id: rs1379512215
• gnomAD v2: 1-1956478-C-T
• gnomAD v3: 1-2025039-C-T
• gnomAD v4: 1-2025039-C-T
• MyVariant Identifiers: chr1:g.1956478C>T (hg19) ; chr1:g.2025039C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2025039C>T , CM000663.2:g.2025039C>T	GRCh38
NC_000001.10:g.1956478C>T , CM000663.1:g.1956478C>T	GRCh37
NC_000001.9:g.1946338C>T	NCBI36
NG_008168.1:g.10711C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.166C>T MANE Select	ENSP00000367848.4:p.Arg56Trp
ENST00000638411.1:c.166C>T	ENSP00000491632.1:p.Arg56Trp
ENST00000638604.1:n.230C>T
ENST00000638771.1:c.166C>T	ENSP00000492435.1:p.Arg56Trp
ENST00000639045.1:c.*152C>T	ENSP00000491997.1:n.*152C>T
ENST00000639777.1:n.770C>T
ENST00000639935.1:n.203C>T
ENST00000640030.1:c.106C>T	ENSP00000491411.1:p.Arg36Trp
ENST00000640067.1:c.166C>T	ENSP00000491844.1:p.Arg56Trp
ENST00000640423.1:n.175C>T
ENST00000640949.1:c.166C>T	ENSP00000492500.1:p.Arg56Trp
ENST00000378585.5:c.166C>T	ENSP00000367848.4:p.Arg56Trp
NM_000815.4:c.166C>T	NP_000806.2:p.Arg56Trp
XM_011541194.1:c.205C>T	XP_011539496.1:p.Arg69Trp
XM_011541194.3:c.205C>T	XP_011539496.1:p.Arg69Trp
XM_017000936.1:c.871C>T	XP_016856425.1:p.Arg291Trp
NM_000815.5:c.166C>T MANE Select	NP_000806.2:p.Arg56Trp