Canonical Allele Identifier: CA439245882
Gene: GABRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.47408886T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406869T>G , CM000666.2:g.47406869T>G GRCh38
NC_000004.11:g.47408886T>G , CM000666.1:g.47408886T>G GRCh37
NC_000004.10:g.47103643T>G NCBI36
NG_051831.1:g.380592T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.1023T>G MANE Select ENSP00000295454.3:p.Ala341=
ENST00000295454.7:c.1023T>G ENSP00000295454.3:p.Ala341=
NM_000812.3:c.1023T>G NP_000803.2:p.Ala341=
XM_011513678.1:c.1002T>G XP_011511980.1:p.Ala334=
XM_017007985.1:c.372T>G XP_016863474.1:p.Ala124=
XM_024453976.1:c.924T>G XP_024309744.1:p.Ala308=
XM_024453977.1:c.924T>G XP_024309745.1:p.Ala308=
XM_024453978.1:c.924T>G XP_024309746.1:p.Ala308=
NM_000812.4:c.1023T>G MANE Select NP_000803.2:p.Ala341=