Canonical Allele Identifier: CA96639381

Gene: GABRA4

Linked Data

• dbSNP Id: rs746885265
• gnomAD v3: 4-46927570-T-C
• gnomAD v4: 4-46927570-T-C
• MyVariant Identifiers: chr4:g.46929587T>C (hg19) ; chr4:g.46927570T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46927570T>C , CM000666.2:g.46927570T>C	GRCh38
NC_000004.11:g.46929587T>C , CM000666.1:g.46929587T>C	GRCh37
NC_000004.10:g.46624344T>C	NCBI36
NG_011809.1:g.70994A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264318.4:c.*655A>G MANE Select	ENSP00000264318.3:n.*655A>G
ENST00000264318.3:c.*655A>G	ENSP00000264318.3:n.*655A>G
NM_000809.3:c.*655A>G	NP_000800.2:n.*655A>G
NM_001204266.1:c.*655A>G	NP_001191195.1:n.*655A>G
NM_001204267.1:c.*655A>G	NP_001191196.1:n.*655A>G
XM_011513677.1:c.*655A>G	XP_011511979.1:n.*655A>G
NM_000809.4:c.*655A>G MANE Select	NP_000800.2:n.*655A>G
NM_001204266.2:c.*655A>G	NP_001191195.1:n.*655A>G
NM_001204267.2:c.*655A>G	NP_001191196.1:n.*655A>G