Canonical Allele Identifier: CA337955324

Gene: GABRD

Linked Data

• ClinVar Variation Id: 1060769
• ClinVar RCV Id: RCV001370241
• dbSNP Id: rs1295769740
• gnomAD v2: 1-1956406-G-A
• gnomAD v3: 1-2024967-G-A
• gnomAD v4: 1-2024967-G-A
• MyVariant Identifiers: chr1:g.1956406G>A (hg19) ; chr1:g.2024967G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2024967G>A , CM000663.2:g.2024967G>A	GRCh38
NC_000001.10:g.1956406G>A , CM000663.1:g.1956406G>A	GRCh37
NC_000001.9:g.1946266G>A	NCBI36
NG_008168.1:g.10639G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.94G>A MANE Select	ENSP00000367848.4:p.Val32Met
ENST00000638411.1:c.94G>A	ENSP00000491632.1:p.Val32Met
ENST00000638604.1:n.158G>A
ENST00000638771.1:c.94G>A	ENSP00000492435.1:p.Val32Met
ENST00000639045.1:c.*80G>A	ENSP00000491997.1:n.*80G>A
ENST00000639777.1:n.698G>A
ENST00000639935.1:n.131G>A
ENST00000640030.1:c.34G>A	ENSP00000491411.1:p.Val12Met
ENST00000640067.1:c.94G>A	ENSP00000491844.1:p.Val32Met
ENST00000640423.1:n.103G>A
ENST00000640949.1:c.94G>A	ENSP00000492500.1:p.Val32Met
ENST00000378585.5:c.94G>A	ENSP00000367848.4:p.Val32Met
NM_000815.4:c.94G>A	NP_000806.2:p.Val32Met
XM_011541194.1:c.133G>A	XP_011539496.1:p.Val45Met
XM_011541194.3:c.133G>A	XP_011539496.1:p.Val45Met
XM_017000936.1:c.799G>A	XP_016856425.1:p.Val267Met
NM_000815.5:c.94G>A MANE Select	NP_000806.2:p.Val32Met