Canonical Allele Identifier: CA2906468
Gene: GABRG1 HGNC NCBI

Linked Data

dbSNP Id: rs200105027
ExAC: 4:46125790 T / G
gnomAD v2: 4-46125790-T-G
gnomAD v3: 4-46123773-T-G
gnomAD v4: 4-46123773-T-G
MyVariant Identifiers: chr4:g.46125790T>G (hg19) chr4:g.46123773T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46123773T>G , CM000666.2:g.46123773T>G GRCh38
NC_000004.11:g.46125790T>G , CM000666.1:g.46125790T>G GRCh37
NC_000004.10:g.45820547T>G NCBI36
NG_046964.1:g.5293A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295452.5:c.104+37A>C MANE Select ENSP00000295452.4:n.104+37A>C
ENST00000295452.4:c.104+37A>C ENSP00000295452.4:n.104+37A>C
NM_173536.3:c.104+37A>C NP_775807.2:n.104+37A>C
NM_173536.4:c.104+37A>C MANE Select NP_775807.2:n.104+37A>C
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