Canonical Allele Identifier: CA439245691
Gene: GABRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.47408718A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406701A>C , CM000666.2:g.47406701A>C GRCh38
NC_000004.11:g.47408718A>C , CM000666.1:g.47408718A>C GRCh37
NC_000004.10:g.47103475A>C NCBI36
NG_051831.1:g.380424A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.855A>C MANE Select ENSP00000295454.3:p.Thr285=
ENST00000295454.7:c.855A>C ENSP00000295454.3:p.Thr285=
NM_000812.3:c.855A>C NP_000803.2:p.Thr285=
XM_011513678.1:c.834A>C XP_011511980.1:p.Thr278=
XM_017007985.1:c.204A>C XP_016863474.1:p.Thr68=
XM_024453976.1:c.756A>C XP_024309744.1:p.Thr252=
XM_024453977.1:c.756A>C XP_024309745.1:p.Thr252=
XM_024453978.1:c.756A>C XP_024309746.1:p.Thr252=
NM_000812.4:c.855A>C MANE Select NP_000803.2:p.Thr285=