Canonical Allele Identifier: CA439245774
Gene: GABRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.47408766T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406749T>A , CM000666.2:g.47406749T>A GRCh38
NC_000004.11:g.47408766T>A , CM000666.1:g.47408766T>A GRCh37
NC_000004.10:g.47103523T>A NCBI36
NG_051831.1:g.380472T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.903T>A MANE Select ENSP00000295454.3:p.Pro301=
ENST00000295454.7:c.903T>A ENSP00000295454.3:p.Pro301=
NM_000812.3:c.903T>A NP_000803.2:p.Pro301=
XM_011513678.1:c.882T>A XP_011511980.1:p.Pro294=
XM_017007985.1:c.252T>A XP_016863474.1:p.Pro84=
XM_024453976.1:c.804T>A XP_024309744.1:p.Pro268=
XM_024453977.1:c.804T>A XP_024309745.1:p.Pro268=
XM_024453978.1:c.804T>A XP_024309746.1:p.Pro268=
NM_000812.4:c.903T>A MANE Select NP_000803.2:p.Pro301=