Canonical Allele Identifier: CA448707876
Gene: TUBB2A HGNC NCBI

Linked Data

gnomAD v4: 6-3154472-C-G
MyVariant Identifiers: chr6:g.3154706C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154472C>G , CM000668.2:g.3154472C>G GRCh38
NC_000006.11:g.3154706C>G , CM000668.1:g.3154706C>G GRCh37
NC_000006.10:g.3099705C>G NCBI36
NG_042223.1:g.8078G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333628.4:c.729G>C MANE Select ENSP00000369703.2:p.Pro243=
ENST00000679400.1:n.785G>C
ENST00000679907.1:n.1117G>C
ENST00000680036.1:n.1511G>C
ENST00000680967.1:n.1819G>C
ENST00000333628.3:c.729G>C ENSP00000369703.2:p.Pro243=
NM_001069.2:c.729G>C NP_001060.1:p.Pro243=
NM_001310315.1:c.474G>C NP_001297244.1:p.Pro158=
NM_001069.3:c.729G>C MANE Select NP_001060.1:p.Pro243=
NM_001310315.2:c.474G>C NP_001297244.1:p.Pro158=