Canonical Allele Identifier: CA2907741
Gene: GABRB1 HGNC NCBI

Linked Data

dbSNP Id: rs151232894
ExAC: 4:47408968 A / C
gnomAD v2: 4-47408968-A-C
MyVariant Identifiers: chr4:g.47408968A>C (hg19) chr4:g.47406951A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406951A>C , CM000666.2:g.47406951A>C GRCh38
NC_000004.11:g.47408968A>C , CM000666.1:g.47408968A>C GRCh37
NC_000004.10:g.47103725A>C NCBI36
NG_051831.1:g.380674A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.1080+25A>C MANE Select ENSP00000295454.3:n.1080+25A>C
ENST00000295454.7:c.1080+25A>C ENSP00000295454.3:n.1080+25A>C
NM_000812.3:c.1080+25A>C NP_000803.2:n.1080+25A>C
XM_011513678.1:c.1059+25A>C XP_011511980.1:n.1059+25A>C
XM_017007985.1:c.429+25A>C XP_016863474.1:n.429+25A>C
XM_024453976.1:c.981+25A>C XP_024309744.1:n.981+25A>C
XM_024453977.1:c.981+25A>C XP_024309745.1:n.981+25A>C
XM_024453978.1:c.981+25A>C XP_024309746.1:n.981+25A>C
NM_000812.4:c.1080+25A>C MANE Select NP_000803.2:n.1080+25A>C
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