Canonical Allele Identifier: CA1267390236

Gene: CD8B

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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