Canonical Allele Identifier: CA1267390235

Gene: CD8B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86817193G= , CM000664.2:g.86817193G=	GRCh38
NC_000002.11:g.87044316G= , CM000664.1:g.87044316G=	GRCh37
NC_000002.10:g.86897827G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331469.6:c.621-1475C=	ENSP00000331172.2:n.621-1475C=
ENST00000349455.7:c.531-1475C=	ENSP00000340592.3:n.531-1475C=
ENST00000393759.6:c.*9-1475C=	ENSP00000377356.2:n.*9-1475C=
ENST00000393761.6:c.494-1475C=	ENSP00000377358.2:n.494-1475C=
NM_001178100.1:c.494-1475C=	NP_001171571.1:n.494-1475C=
NM_172101.3:c.*9-1475C=	NP_742099.1:n.*9-1475C=
NM_172102.3:c.531-1475C=	NP_742100.1:n.531-1475C=
NM_172213.3:c.621-1475C=	NP_757362.1:n.621-1475C=
XR_940321.1:n.1609-3996G=
XR_940321.2:n.1609-3996G=
NM_172101.4:c.*9-1475C=	NP_742099.1:n.*9-1475C=
NM_172102.4:c.531-1475C=	NP_742100.1:n.531-1475C=
NM_172213.4:c.621-1475C=	NP_757362.1:n.621-1475C=
NM_001178100.2:c.494-1475C=	NP_001171571.1:n.494-1475C=
NM_172101.5:c.*9-1475C=	NP_742099.1:n.*9-1475C=
NM_172102.5:c.531-1475C=	NP_742100.1:n.531-1475C=
NM_172213.5:c.621-1475C=	NP_757362.1:n.621-1475C=