Canonical Allele Identifier: CA795412941

Gene: GABRA4

Linked Data

• dbSNP Id: rs1473838579
• gnomAD v3: 4-46993532-C-T
• gnomAD v4: 4-46993532-C-T
• MyVariant Identifiers: chr4:g.46995549C>T (hg19) ; chr4:g.46993532C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993532C>T , CM000666.2:g.46993532C>T	GRCh38
NC_000004.11:g.46995549C>T , CM000666.1:g.46995549C>T	GRCh37
NC_000004.10:g.46690306C>T	NCBI36
NG_011809.1:g.5032G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.-108G>A MANE Select	ENSP00000264318.3:n.-108G>A
ENST00000264318.3:c.-108G>A	ENSP00000264318.3:n.-108G>A
ENST00000502874.1:c.-108G>A	ENSP00000424386.1:n.-108G>A
ENST00000509316.1:n.17G>A
NM_000809.3:c.-108G>A	NP_000800.2:n.-108G>A
XM_011513677.1:c.-108G>A	XP_011511979.1:n.-108G>A
NM_000809.4:c.-108G>A MANE Select	NP_000800.2:n.-108G>A
NM_001204266.2:c.-97G>A	NP_001191195.1:n.-97G>A
NM_001204267.2:c.-97G>A	NP_001191196.1:n.-97G>A