Canonical Allele Identifier: CA96639389
Gene: GABRA4 HGNC NCBI

Linked Data

dbSNP Id: rs41307145
MyVariant Identifiers: chr4:g.46929639G>C (hg19) chr4:g.46927622G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46927622G>C , CM000666.2:g.46927622G>C GRCh38
NC_000004.11:g.46929639G>C , CM000666.1:g.46929639G>C GRCh37
NC_000004.10:g.46624396G>C NCBI36
NG_011809.1:g.70942C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264318.4:c.*603C>G MANE Select ENSP00000264318.3:n.*603C>G
ENST00000264318.3:c.*603C>G ENSP00000264318.3:n.*603C>G
NM_000809.3:c.*603C>G NP_000800.2:n.*603C>G
NM_001204266.1:c.*603C>G NP_001191195.1:n.*603C>G
NM_001204267.1:c.*603C>G NP_001191196.1:n.*603C>G
XM_011513677.1:c.*603C>G XP_011511979.1:n.*603C>G
NM_000809.4:c.*603C>G MANE Select NP_000800.2:n.*603C>G
NM_001204266.2:c.*603C>G NP_001191195.1:n.*603C>G
NM_001204267.2:c.*603C>G NP_001191196.1:n.*603C>G
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