Canonical Allele Identifier: CA449868020

Linked Data

MyVariant Identifiers: chr6:g.33543116C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33575339C>A , CM000668.2:g.33575339C>A GRCh38
NC_000006.11:g.33543116C>A , CM000668.1:g.33543116C>A GRCh37
NC_000006.10:g.33651094C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374467.4:c.309G>T (BAK1) MANE Select ENSP00000363591.3:p.Thr103=
ENST00000360661.9:c.249G>T (BAK1) ENSP00000353878.6:p.Thr83=
ENST00000374467.3:c.309G>T (BAK1) ENSP00000363591.3:p.Thr103=
ENST00000442998.6:c.309G>T (BAK1) ENSP00000391258.2:p.Thr103=
ENST00000612409.1:n.249-12C>A (GGNBP1)
NM_001188.3:c.309G>T (BAK1) NP_001179.1:p.Thr103=
XM_011514779.1:c.309G>T (BAK1) XP_011513081.1:p.Thr103=
XM_011514780.1:c.132G>T (BAK1) XP_011513082.1:p.Thr44=
XM_011514779.3:c.309G>T (BAK1) XP_011513081.1:p.Thr103=
NM_001188.4:c.309G>T (BAK1) MANE Select NP_001179.1:p.Thr103=