Canonical Allele Identifier: CA1149429751

Gene: GABRD

Linked Data

• dbSNP Id: rs1658872554
• gnomAD v4: 1-2024760-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2024760T>C , CM000663.2:g.2024760T>C	GRCh38
NC_000001.10:g.1956199T>C , CM000663.1:g.1956199T>C	GRCh37
NC_000001.9:g.1946059T>C	NCBI36
NG_008168.1:g.10432T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.69-182T>C MANE Select	ENSP00000367848.4:n.69-182T>C
ENST00000638411.1:c.69-182T>C	ENSP00000491632.1:n.69-182T>C
ENST00000638604.1:n.133-182T>C
ENST00000638771.1:c.69-182T>C	ENSP00000492435.1:n.69-182T>C
ENST00000639045.1:c.*55-182T>C	ENSP00000491997.1:n.*55-182T>C
ENST00000639777.1:n.491T>C
ENST00000639935.1:n.106-182T>C
ENST00000640030.1:c.9-182T>C	ENSP00000491411.1:n.9-182T>C
ENST00000640067.1:c.69-182T>C	ENSP00000491844.1:n.69-182T>C
ENST00000640423.1:n.78-182T>C
ENST00000640949.1:c.69-182T>C	ENSP00000492500.1:n.69-182T>C
ENST00000378585.5:c.69-182T>C	ENSP00000367848.4:n.69-182T>C
NM_000815.4:c.69-182T>C	NP_000806.2:n.69-182T>C
XM_011541194.1:c.108-182T>C	XP_011539496.1:n.108-182T>C
XM_011541194.3:c.108-182T>C	XP_011539496.1:n.108-182T>C
XM_017000936.1:c.592T>C	XP_016856425.1:p.Phe198Leu
NM_000815.5:c.69-182T>C MANE Select	NP_000806.2:n.69-182T>C