Canonical Allele Identifier: CA439245682
Gene: GABRB1 HGNC NCBI

Linked Data

gnomAD v4: 4-47406689-G-T
MyVariant Identifiers: chr4:g.47408706G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406689G>T , CM000666.2:g.47406689G>T GRCh38
NC_000004.11:g.47408706G>T , CM000666.1:g.47408706G>T GRCh37
NC_000004.10:g.47103463G>T NCBI36
NG_051831.1:g.380412G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.843G>T MANE Select ENSP00000295454.3:p.Thr281=
ENST00000295454.7:c.843G>T ENSP00000295454.3:p.Thr281=
NM_000812.3:c.843G>T NP_000803.2:p.Thr281=
XM_011513678.1:c.822G>T XP_011511980.1:p.Thr274=
XM_017007985.1:c.192G>T XP_016863474.1:p.Thr64=
XM_024453976.1:c.744G>T XP_024309744.1:p.Thr248=
XM_024453977.1:c.744G>T XP_024309745.1:p.Thr248=
XM_024453978.1:c.744G>T XP_024309746.1:p.Thr248=
NM_000812.4:c.843G>T MANE Select NP_000803.2:p.Thr281=