Canonical Allele Identifier: CA439245698
Gene: GABRB1 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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