Canonical Allele Identifier: CA363589114

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810476C>G (hg19) ; chr6:g.32842699C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842699C>G , CM000668.2:g.32842699C>G	GRCh38
NC_000006.11:g.32810476C>G , CM000668.1:g.32810476C>G	GRCh37
NC_000006.10:g.32918454C>G	NCBI36
NG_009793.3:g.1072G>C
NG_028165.1:g.7237G>C
NG_009793.4:g.1072G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.559G>C
ENST00000697612.1:n.1237G>C
ENST00000374881.3:c.368G>C	ENSP00000364015.2:p.Trp123Ser
ENST00000374882.8:c.380G>C MANE Select	ENSP00000364016.4:p.Trp127Ser
ENST00000650411.1:n.1701G>C
ENST00000650793.1:n.559G>C
ENST00000374881.2:c.368G>C	ENSP00000364015.2:p.Trp123Ser
ENST00000374882.7:c.380G>C	ENSP00000364016.3:p.Trp127Ser
ENST00000395339.7:c.308G>C	ENSP00000378748.3:p.Trp103Ser
ENST00000484003.1:n.764G>C
NM_004159.4:c.368G>C	NP_004150.1:p.Trp123Ser
NM_148919.3:c.380G>C	NP_683720.2:p.Trp127Ser
NM_148919.4:c.380G>C MANE Select	NP_683720.2:p.Trp127Ser
NM_004159.5:c.368G>C	NP_004150.1:p.Trp123Ser