Canonical Allele Identifier: CA823881032

Gene: HLA-B

Linked Data

• dbSNP Id: rs1227184735
• MyVariant Identifiers: chr6:g.31324369_31324371del (hg19) ; chr6:g.31356592_31356594del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356592_31356594del , CM000668.2:g.31356592_31356594del	GRCh38
NC_000006.11:g.31324369_31324371del , CM000668.1:g.31324369_31324371del	GRCh37
NC_000006.10:g.31432348_31432350del	NCBI36
NG_023187.1:g.5619_5621del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1816+94_1816+96del
ENST00000481849.6:n.1816+94_1816+96del
ENST00000497377.6:n.1816+94_1816+96del
ENST00000640094.2:c.343+94_343+96del	ENSP00000491275.2:n.343+94_343+96del
ENST00000696558.1:c.343+94_343+96del	ENSP00000512716.1:n.343+94_343+96del
ENST00000696559.1:c.343+94_343+96del	ENSP00000512717.1:n.343+94_343+96del
ENST00000696560.1:c.343+94_343+96del	ENSP00000512718.1:n.343+94_343+96del
ENST00000696561.1:c.343+94_343+96del	ENSP00000512719.1:n.343+94_343+96del
ENST00000696562.1:c.343+94_343+96del	ENSP00000512720.1:n.343+94_343+96del
ENST00000412585.7:c.343+94_343+96del MANE Select	ENSP00000399168.2:n.343+94_343+96del
ENST00000412585.6:c.343+94_343+96del	ENSP00000399168.2:n.343+94_343+96del
ENST00000434333.1:c.376+94_376+96del	ENSP00000405931.1:n.376+94_376+96del
ENST00000474381.1:n.218+94_218+96del
ENST00000498007.1:n.458_460del
NM_005514.6:c.343+94_343+96del	NP_005505.2:n.343+94_343+96del
XM_011514556.1:c.376+94_376+96del	XP_011512858.1:n.376+94_376+96del
XM_011514557.1:c.343+94_343+96del	XP_011512859.1:n.343+94_343+96del
XR_926175.1:n.353+94_353+96del
NM_005514.7:c.343+94_343+96del	NP_005505.2:n.343+94_343+96del
NM_005514.8:c.343+94_343+96del MANE Select	NP_005505.2:n.343+94_343+96del