Canonical Allele Identifier: CA449791977

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356790-GC-G
• COSMIC: COSM1443268
• MyVariant Identifiers: chr6:g.31324568del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356794del , CM000668.2:g.31356794del	GRCh38
NC_000006.11:g.31324571del , CM000668.1:g.31324571del	GRCh37
NC_000006.10:g.31432550del	NCBI36
NG_023187.1:g.5422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1713del
ENST00000481849.6:n.1713del
ENST00000497377.6:n.1713del
ENST00000640094.2:c.240del	ENSP00000491275.2:p.Pro81ArgfsTer?
ENST00000696558.1:c.240del	ENSP00000512716.1:p.Pro81ArgfsTer?
ENST00000696559.1:c.240del	ENSP00000512717.1:p.Pro81ArgfsTer?
ENST00000696560.1:c.240del	ENSP00000512718.1:p.Pro81ArgfsTer?
ENST00000696561.1:c.240del	ENSP00000512719.1:p.Pro81ArgfsTer?
ENST00000696562.1:c.240del	ENSP00000512720.1:p.Pro81ArgfsTer?
ENST00000412585.7:c.240del MANE Select	ENSP00000399168.2:p.Pro81ArgfsTer?
ENST00000412585.6:c.240del	ENSP00000399168.2:p.Pro81ArgfsTer?
ENST00000434333.1:c.273del	ENSP00000405931.1:p.Pro92ArgfsTer?
ENST00000474381.1:n.115del
ENST00000498007.1:n.261del
ENST00000603274.1:n.148del
NM_005514.6:c.240del	NP_005505.2:p.Pro81ArgfsTer?
XM_011514556.1:c.273del	XP_011512858.1:p.Pro92ArgfsTer?
XM_011514557.1:c.240del	XP_011512859.1:p.Pro81ArgfsTer?
XR_926175.1:n.250del
NM_005514.7:c.240del	NP_005505.2:p.Pro81ArgfsTer?
NM_005514.8:c.240del MANE Select	NP_005505.2:p.Pro81ArgfsTer?