Canonical Allele Identifier: CA439236971
Gene: GABRG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.46125868C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46123851C>G , CM000666.2:g.46123851C>G GRCh38
NC_000004.11:g.46125868C>G , CM000666.1:g.46125868C>G GRCh37
NC_000004.10:g.45820625C>G NCBI36
NG_046964.1:g.5215G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295452.5:c.63G>C MANE Select ENSP00000295452.4:p.Val21=
ENST00000295452.4:c.63G>C ENSP00000295452.4:p.Val21=
NM_173536.3:c.63G>C NP_775807.2:p.Val21=
NM_173536.4:c.63G>C MANE Select NP_775807.2:p.Val21=
Search 100 bp 5'
Search 100 bp 3'