Canonical Allele Identifier: CA1455320242
Gene: GABRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406526_47406527delinsCA , CM000666.2:g.47406526_47406527delinsCA GRCh38
NC_000004.11:g.47408543_47408544delinsCA , CM000666.1:g.47408543_47408544delinsCA GRCh37
NC_000004.10:g.47103300_47103301delinsCA NCBI36
NG_051831.1:g.380249_380250delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.836-156_836-155delinsCA MANE Select ENSP00000295454.3:n.836-156_836-155delinsCA
ENST00000295454.7:c.836-156_836-155delinsCA ENSP00000295454.3:n.836-156_836-155delinsCA
NM_000812.3:c.836-156_836-155delinsCA NP_000803.2:n.836-156_836-155delinsCA
XM_011513678.1:c.815-156_815-155delinsCA XP_011511980.1:n.815-156_815-155delinsCA
XM_017007985.1:c.185-156_185-155delinsCA XP_016863474.1:n.185-156_185-155delinsCA
XM_024453976.1:c.737-156_737-155delinsCA XP_024309744.1:n.737-156_737-155delinsCA
XM_024453977.1:c.737-156_737-155delinsCA XP_024309745.1:n.737-156_737-155delinsCA
XM_024453978.1:c.737-156_737-155delinsCA XP_024309746.1:n.737-156_737-155delinsCA
NM_000812.4:c.836-156_836-155delinsCA MANE Select NP_000803.2:n.836-156_836-155delinsCA