Canonical Allele Identifier: CA1455320319
Gene: GABRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406604_47406605delinsTG , CM000666.2:g.47406604_47406605delinsTG GRCh38
NC_000004.11:g.47408621_47408622delinsTG , CM000666.1:g.47408621_47408622delinsTG GRCh37
NC_000004.10:g.47103378_47103379delinsTG NCBI36
NG_051831.1:g.380327_380328delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.836-78_836-77delinsTG MANE Select ENSP00000295454.3:n.836-78_836-77delinsTG
ENST00000295454.7:c.836-78_836-77delinsTG ENSP00000295454.3:n.836-78_836-77delinsTG
NM_000812.3:c.836-78_836-77delinsTG NP_000803.2:n.836-78_836-77delinsTG
XM_011513678.1:c.815-78_815-77delinsTG XP_011511980.1:n.815-78_815-77delinsTG
XM_017007985.1:c.185-78_185-77delinsTG XP_016863474.1:n.185-78_185-77delinsTG
XM_024453976.1:c.737-78_737-77delinsTG XP_024309744.1:n.737-78_737-77delinsTG
XM_024453977.1:c.737-78_737-77delinsTG XP_024309745.1:n.737-78_737-77delinsTG
XM_024453978.1:c.737-78_737-77delinsTG XP_024309746.1:n.737-78_737-77delinsTG
NM_000812.4:c.836-78_836-77delinsTG MANE Select NP_000803.2:n.836-78_836-77delinsTG