Canonical Allele Identifier: CA449868038

Linked Data

MyVariant Identifiers: chr6:g.33543128G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33575351G>A , CM000668.2:g.33575351G>A GRCh38
NC_000006.11:g.33543128G>A , CM000668.1:g.33543128G>A GRCh37
NC_000006.10:g.33651106G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374467.4:c.297C>T (BAK1) MANE Select ENSP00000363591.3:p.His99=
ENST00000360661.9:c.237C>T (BAK1) ENSP00000353878.6:p.His79=
ENST00000374467.3:c.297C>T (BAK1) ENSP00000363591.3:p.His99=
ENST00000442998.6:c.297C>T (BAK1) ENSP00000391258.2:p.His99=
ENST00000612409.1:n.249G>A (GGNBP1)
NM_001188.3:c.297C>T (BAK1) NP_001179.1:p.His99=
XM_011514779.1:c.297C>T (BAK1) XP_011513081.1:p.His99=
XM_011514780.1:c.120C>T (BAK1) XP_011513082.1:p.His40=
XM_011514779.3:c.297C>T (BAK1) XP_011513081.1:p.His99=
NM_001188.4:c.297C>T (BAK1) MANE Select NP_001179.1:p.His99=