Canonical Allele Identifier: CA449832561

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810511G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842734G>C , CM000668.2:g.32842734G>C	GRCh38
NC_000006.11:g.32810511G>C , CM000668.1:g.32810511G>C	GRCh37
NC_000006.10:g.32918489G>C	NCBI36
NG_009793.3:g.1037C>G
NG_028165.1:g.7202C>G
NG_009793.4:g.1037C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.524C>G
ENST00000697612.1:n.1202C>G
ENST00000374881.3:c.333C>G	ENSP00000364015.2:p.Gly111=
ENST00000374882.8:c.345C>G MANE Select	ENSP00000364016.4:p.Gly115=
ENST00000650411.1:n.1666C>G
ENST00000650793.1:n.524C>G
ENST00000374881.2:c.333C>G	ENSP00000364015.2:p.Gly111=
ENST00000374882.7:c.345C>G	ENSP00000364016.3:p.Gly115=
ENST00000395339.7:c.296-23C>G	ENSP00000378748.3:n.296-23C>G
ENST00000484003.1:n.729C>G
NM_004159.4:c.333C>G	NP_004150.1:p.Gly111=
NM_148919.3:c.345C>G	NP_683720.2:p.Gly115=
NM_148919.4:c.345C>G MANE Select	NP_683720.2:p.Gly115=
NM_004159.5:c.333C>G	NP_004150.1:p.Gly111=