Canonical Allele Identifier: CA795333292
Gene: GABRG1 HGNC NCBI

Linked Data

dbSNP Id: rs1257804421
gnomAD v3: 4-46123667-G-C
gnomAD v4: 4-46123667-G-C
MyVariant Identifiers: chr4:g.46125684G>C (hg19) chr4:g.46123667G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46123667G>C , CM000666.2:g.46123667G>C GRCh38
NC_000004.11:g.46125684G>C , CM000666.1:g.46125684G>C GRCh37
NC_000004.10:g.45820441G>C NCBI36
NG_046964.1:g.5399C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295452.5:c.104+143C>G MANE Select ENSP00000295452.4:n.104+143C>G
ENST00000295452.4:c.104+143C>G ENSP00000295452.4:n.104+143C>G
NM_173536.3:c.104+143C>G NP_775807.2:n.104+143C>G
NM_173536.4:c.104+143C>G MANE Select NP_775807.2:n.104+143C>G
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