Canonical Allele Identifier: CA15314018
Gene: GABRA2 HGNC NCBI

Linked Data

dbSNP Id: rs497068

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46248660G>A , CM000666.2:g.46248660G>A GRCh38
NC_000004.11:g.46250677G>A , CM000666.1:g.46250677G>A GRCh37
NC_000004.10:g.45945434G>A NCBI36
NG_012835.1:g.146380C>T
NG_012835.2:g.146380C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381620.9:c.*1648C>T MANE Select ENSP00000371033.4:n.*1648C>T
ENST00000510861.5:c.*1648C>T ENSP00000421828.1:n.*1648C>T
ENST00000514090.5:c.*1648C>T ENSP00000421300.1:n.*1648C>T
XM_005248080.2:c.*1648C>T XP_005248137.1:n.*1648C>T
XM_011513675.1:c.*1648C>T XP_011511977.1:n.*1648C>T
XM_011513676.1:c.*1648C>T XP_011511978.1:n.*1648C>T
NM_000807.3:c.*1648C>T NP_000798.2:n.*1648C>T
NM_001114175.2:c.*1648C>T NP_001107647.1:n.*1648C>T
NM_001286827.2:c.*1648C>T NP_001273756.1:n.*1648C>T
NM_001330690.1:c.*1648C>T NP_001317619.1:n.*1648C>T
XM_017007982.2:c.*1648C>T XP_016863471.1:n.*1648C>T
XM_017007983.2:c.*1648C>T XP_016863472.1:n.*1648C>T
XM_024453963.1:c.*1648C>T XP_024309731.1:n.*1648C>T
XM_024453964.1:c.*1648C>T XP_024309732.1:n.*1648C>T
XM_024453965.1:c.*1648C>T XP_024309733.1:n.*1648C>T
XM_024453966.1:c.*1648C>T XP_024309734.1:n.*1648C>T
XM_024453967.1:c.*1648C>T XP_024309735.1:n.*1648C>T
XM_024453968.1:c.*1648C>T XP_024309736.1:n.*1648C>T
XM_024453969.1:c.*1648C>T XP_024309737.1:n.*1648C>T
XM_024453970.1:c.*1648C>T XP_024309738.1:n.*1648C>T
XM_024453971.1:c.*1648C>T XP_024309739.1:n.*1648C>T
XM_024453972.1:c.*1648C>T XP_024309740.1:n.*1648C>T
XM_024453973.1:c.*1648C>T XP_024309741.1:n.*1648C>T
XM_024453974.1:c.*1648C>T XP_024309742.1:n.*1648C>T
NM_000807.4:c.*1648C>T MANE Select NP_000798.2:n.*1648C>T
NM_001114175.3:c.*1648C>T NP_001107647.1:n.*1648C>T
NM_001286827.3:c.*1648C>T NP_001273756.1:n.*1648C>T
NM_001330690.2:c.*1648C>T NP_001317619.1:n.*1648C>T
NM_001377144.1:c.*1648C>T NP_001364073.1:n.*1648C>T
NM_001377145.1:c.*1648C>T NP_001364074.1:n.*1648C>T
NM_001377146.1:c.*1648C>T NP_001364075.1:n.*1648C>T
NM_001377147.1:c.*1648C>T NP_001364076.1:n.*1648C>T
NM_001377148.1:c.*1648C>T NP_001364077.1:n.*1648C>T
NM_001377149.1:c.*1648C>T NP_001364078.1:n.*1648C>T
NM_001377150.1:c.*1648C>T NP_001364079.1:n.*1648C>T
NM_001377151.1:c.*1648C>T NP_001364080.1:n.*1648C>T
NM_001377152.1:c.*1648C>T NP_001364081.1:n.*1648C>T
NM_001377153.1:c.*1648C>T NP_001364082.1:n.*1648C>T
NM_001377154.1:c.*1648C>T NP_001364083.1:n.*1648C>T