Canonical Allele Identifier: CA439245908
Gene: GABRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.47408919T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406902T>C , CM000666.2:g.47406902T>C GRCh38
NC_000004.11:g.47408919T>C , CM000666.1:g.47408919T>C GRCh37
NC_000004.10:g.47103676T>C NCBI36
NG_051831.1:g.380625T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.1056T>C MANE Select ENSP00000295454.3:p.Asn352=
ENST00000295454.7:c.1056T>C ENSP00000295454.3:p.Asn352=
NM_000812.3:c.1056T>C NP_000803.2:p.Asn352=
XM_011513678.1:c.1035T>C XP_011511980.1:p.Asn345=
XM_017007985.1:c.405T>C XP_016863474.1:p.Asn135=
XM_024453976.1:c.957T>C XP_024309744.1:p.Asn319=
XM_024453977.1:c.957T>C XP_024309745.1:p.Asn319=
XM_024453978.1:c.957T>C XP_024309746.1:p.Asn319=
NM_000812.4:c.1056T>C MANE Select NP_000803.2:p.Asn352=