Canonical Allele Identifier: CA439236997
Gene: GABRG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.46125901G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46123884G>C , CM000666.2:g.46123884G>C GRCh38
NC_000004.11:g.46125901G>C , CM000666.1:g.46125901G>C GRCh37
NC_000004.10:g.45820658G>C NCBI36
NG_046964.1:g.5182C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295452.5:c.30C>G MANE Select ENSP00000295452.4:p.Ser10=
ENST00000295452.4:c.30C>G ENSP00000295452.4:p.Ser10=
NM_173536.3:c.30C>G NP_775807.2:p.Ser10=
NM_173536.4:c.30C>G MANE Select NP_775807.2:p.Ser10=