Canonical Allele Identifier: CA439245697
Gene: GABRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.47408727C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406710C>G , CM000666.2:g.47406710C>G GRCh38
NC_000004.11:g.47408727C>G , CM000666.1:g.47408727C>G GRCh37
NC_000004.10:g.47103484C>G NCBI36
NG_051831.1:g.380433C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295454.8:c.864C>G MANE Select ENSP00000295454.3:p.Thr288=
ENST00000295454.7:c.864C>G ENSP00000295454.3:p.Thr288=
NM_000812.3:c.864C>G NP_000803.2:p.Thr288=
XM_011513678.1:c.843C>G XP_011511980.1:p.Thr281=
XM_017007985.1:c.213C>G XP_016863474.1:p.Thr71=
XM_024453976.1:c.765C>G XP_024309744.1:p.Thr255=
XM_024453977.1:c.765C>G XP_024309745.1:p.Thr255=
XM_024453978.1:c.765C>G XP_024309746.1:p.Thr255=
NM_000812.4:c.864C>G MANE Select NP_000803.2:p.Thr288=