Canonical Allele Identifier: CA823882656

Gene: HLA-B

Linked Data

• dbSNP Id: rs1456744326
• MyVariant Identifiers: chr6:g.31324909_31324911del (hg19) ; chr6:g.31357132_31357134del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357133_31357135del , CM000668.2:g.31357133_31357135del	GRCh38
NC_000006.11:g.31324910_31324912del , CM000668.1:g.31324910_31324912del	GRCh37
NC_000006.10:g.31432889_31432891del	NCBI36
NG_023187.1:g.5079_5081del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1498_1500del
ENST00000481849.6:n.1498_1500del
ENST00000497377.6:n.1498_1500del
ENST00000640094.2:c.25_27del	ENSP00000491275.2:p.Val9del
ENST00000696558.1:c.25_27del	ENSP00000512716.1:p.Val9del
ENST00000696559.1:c.25_27del	ENSP00000512717.1:p.Val9del
ENST00000696560.1:c.25_27del	ENSP00000512718.1:p.Val9del
ENST00000696561.1:c.25_27del	ENSP00000512719.1:p.Val9del
ENST00000696562.1:c.25_27del	ENSP00000512720.1:p.Val9del
ENST00000412585.7:c.25_27del MANE Select	ENSP00000399168.2:p.Val9del
ENST00000412585.6:c.25_27del	ENSP00000399168.2:p.Val9del
ENST00000434333.1:c.-71_-69del	ENSP00000405931.1:n.-71_-69del
ENST00000498007.1:n.46_48del
ENST00000603274.1:n.487_489del
NM_005514.6:c.25_27del	NP_005505.2:p.Val9del
XM_011514557.1:c.25_27del	XP_011512859.1:p.Val9del
XR_926175.1:n.35_37del
NM_005514.7:c.25_27del	NP_005505.2:p.Val9del
NM_005514.8:c.25_27del MANE Select	NP_005505.2:p.Val9del