Canonical Allele Identifier: CA97039411
Gene: GABRG1 HGNC NCBI

Linked Data

dbSNP Id: rs941754058
MyVariant Identifiers: chr4:g.46125845G>T (hg19) chr4:g.46123828G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46123828G>T , CM000666.2:g.46123828G>T GRCh38
NC_000004.11:g.46125845G>T , CM000666.1:g.46125845G>T GRCh37
NC_000004.10:g.45820602G>T NCBI36
NG_046964.1:g.5238C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295452.5:c.86C>A MANE Select ENSP00000295452.4:p.Thr29Asn
ENST00000295452.4:c.86C>A ENSP00000295452.4:p.Thr29Asn
NM_173536.3:c.86C>A NP_775807.2:p.Thr29Asn
NM_173536.4:c.86C>A MANE Select NP_775807.2:p.Thr29Asn
Search 100 bp 5'
Search 100 bp 3'