Canonical Allele Identifier: CA795448986
Gene: GABRA4 HGNC NCBI

Linked Data

dbSNP Id: rs1388697425
MyVariant Identifiers: chr4:g.46929654C>T (hg19) chr4:g.46927637C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46927637C>T , CM000666.2:g.46927637C>T GRCh38
NC_000004.11:g.46929654C>T , CM000666.1:g.46929654C>T GRCh37
NC_000004.10:g.46624411C>T NCBI36
NG_011809.1:g.70927G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264318.4:c.*588G>A MANE Select ENSP00000264318.3:n.*588G>A
ENST00000264318.3:c.*588G>A ENSP00000264318.3:n.*588G>A
NM_000809.3:c.*588G>A NP_000800.2:n.*588G>A
NM_001204266.1:c.*588G>A NP_001191195.1:n.*588G>A
NM_001204267.1:c.*588G>A NP_001191196.1:n.*588G>A
XM_011513677.1:c.*588G>A XP_011511979.1:n.*588G>A
NM_000809.4:c.*588G>A MANE Select NP_000800.2:n.*588G>A
NM_001204266.2:c.*588G>A NP_001191195.1:n.*588G>A
NM_001204267.2:c.*588G>A NP_001191196.1:n.*588G>A
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