Canonical Allele Identifier: CA439245820
Gene: GABRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.47408820G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406803G>C , CM000666.2:g.47406803G>C GRCh38
NC_000004.11:g.47408820G>C , CM000666.1:g.47408820G>C GRCh37
NC_000004.10:g.47103577G>C NCBI36
NG_051831.1:g.380526G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.957G>C MANE Select ENSP00000295454.3:p.Leu319=
ENST00000295454.7:c.957G>C ENSP00000295454.3:p.Leu319=
NM_000812.3:c.957G>C NP_000803.2:p.Leu319=
XM_011513678.1:c.936G>C XP_011511980.1:p.Leu312=
XM_017007985.1:c.306G>C XP_016863474.1:p.Leu102=
XM_024453976.1:c.858G>C XP_024309744.1:p.Leu286=
XM_024453977.1:c.858G>C XP_024309745.1:p.Leu286=
XM_024453978.1:c.858G>C XP_024309746.1:p.Leu286=
NM_000812.4:c.957G>C MANE Select NP_000803.2:p.Leu319=