Canonical Allele Identifier: CA3711214

Gene: HLA-B

Linked Data

• dbSNP Id: rs745606779
• ExAC: 6:31322403 CACTT / C
• gnomAD v2: 6-31322403-CACTT-C
• gnomAD v4: 6-31354626-CACTT-C
• MyVariant Identifiers: chr6:g.31322404_31322407del (hg19) ; chr6:g.31354627_31354630del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354629_31354632del , CM000668.2:g.31354629_31354632del	GRCh38
NC_000006.11:g.31322406_31322409del , CM000668.1:g.31322406_31322409del	GRCh37
NC_000006.10:g.31430385_31430388del	NCBI36
NG_023187.1:g.7583_7586del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3092+3_3092+6del
ENST00000481849.6:n.3052+3_3052+6del
ENST00000497377.6:n.2959+3_2959+6del
ENST00000640094.2:c.928+3_928+6del	ENSP00000491275.2:n.928+3_928+6del
ENST00000696558.1:c.1114+3_1114+6del	ENSP00000512716.1:n.1114+3_1114+6del
ENST00000696559.1:c.1045+3_1045+6del	ENSP00000512717.1:n.1045+3_1045+6del
ENST00000696560.1:c.1045+3_1045+6del	ENSP00000512718.1:n.1045+3_1045+6del
ENST00000696561.1:c.1045+3_1045+6del	ENSP00000512719.1:n.1045+3_1045+6del
ENST00000696562.1:c.1045+3_1045+6del	ENSP00000512720.1:n.1045+3_1045+6del
ENST00000412585.7:c.1045+3_1045+6del MANE Select	ENSP00000399168.2:n.1045+3_1045+6del
ENST00000640094.1:c.121+3_121+6del	ENSP00000491275.1:n.121+3_121+6del
ENST00000412585.6:c.1045+3_1045+6del	ENSP00000399168.2:n.1045+3_1045+6del
ENST00000481849.5:n.177_180del
ENST00000497377.5:n.444+3_444+6del
NM_005514.6:c.1045+3_1045+6del	NP_005505.2:n.1045+3_1045+6del
XM_011514556.1:c.1078+3_1078+6del	XP_011512858.1:n.1078+3_1078+6del
XM_011514557.1:c.928+3_928+6del	XP_011512859.1:n.928+3_928+6del
XR_926175.1:n.1484+3_1484+6del
NM_005514.7:c.1045+3_1045+6del	NP_005505.2:n.1045+3_1045+6del
NM_005514.8:c.1045+3_1045+6del MANE Select	NP_005505.2:n.1045+3_1045+6del