Canonical Allele Identifier: CA439245900
Gene: GABRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1270829797
gnomAD v2: 4-47408907-C-G
gnomAD v4: 4-47406890-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406890C>G , CM000666.2:g.47406890C>G GRCh38
NC_000004.11:g.47408907C>G , CM000666.1:g.47408907C>G GRCh37
NC_000004.10:g.47103664C>G NCBI36
NG_051831.1:g.380613C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.1044C>G MANE Select ENSP00000295454.3:p.Ala348=
ENST00000295454.7:c.1044C>G ENSP00000295454.3:p.Ala348=
NM_000812.3:c.1044C>G NP_000803.2:p.Ala348=
XM_011513678.1:c.1023C>G XP_011511980.1:p.Ala341=
XM_017007985.1:c.393C>G XP_016863474.1:p.Ala131=
XM_024453976.1:c.945C>G XP_024309744.1:p.Ala315=
XM_024453977.1:c.945C>G XP_024309745.1:p.Ala315=
XM_024453978.1:c.945C>G XP_024309746.1:p.Ala315=
NM_000812.4:c.1044C>G MANE Select NP_000803.2:p.Ala348=