Canonical Allele Identifier: CA11686850
Gene: GABRA4 HGNC NCBI
GABRB1 HGNC NCBI

Linked Data

dbSNP Id: rs13151759
gnomAD v2: 4-46995653-G-T
gnomAD v3: 4-46993636-G-T
gnomAD v4: 4-46993636-G-T
MyVariant Identifiers: chr4:g.46995653G>T (hg19) chr4:g.46993636G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46993636G>T , CM000666.2:g.46993636G>T GRCh38
NC_000004.11:g.46995653G>T , CM000666.1:g.46995653G>T GRCh37
NC_000004.10:g.46690410G>T NCBI36
NG_011809.1:g.4928C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.3:c.-212C>A (GABRA4) ENSP00000264318.3:n.-212C>A
NM_000809.3:c.-212C>A (GABRA4) NP_000800.2:n.-212C>A
XM_011513677.1:c.-212C>A (GABRA4) XP_011511979.1:n.-212C>A
XM_024453977.1:c.-382G>T (GABRB1) XP_024309745.1:n.-382G>T
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