Canonical Allele Identifier: CA449868027

Linked Data

MyVariant Identifiers: chr6:g.33543122C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33575345C>T , CM000668.2:g.33575345C>T GRCh38
NC_000006.11:g.33543122C>T , CM000668.1:g.33543122C>T GRCh37
NC_000006.10:g.33651100C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374467.4:c.303G>A (BAK1) MANE Select ENSP00000363591.3:p.Gln101=
ENST00000360661.9:c.243G>A (BAK1) ENSP00000353878.6:p.Gln81=
ENST00000374467.3:c.303G>A (BAK1) ENSP00000363591.3:p.Gln101=
ENST00000442998.6:c.303G>A (BAK1) ENSP00000391258.2:p.Gln101=
ENST00000612409.1:n.249-6C>T (GGNBP1)
NM_001188.3:c.303G>A (BAK1) NP_001179.1:p.Gln101=
XM_011514779.1:c.303G>A (BAK1) XP_011513081.1:p.Gln101=
XM_011514780.1:c.126G>A (BAK1) XP_011513082.1:p.Gln42=
XM_011514779.3:c.303G>A (BAK1) XP_011513081.1:p.Gln101=
NM_001188.4:c.303G>A (BAK1) MANE Select NP_001179.1:p.Gln101=