Canonical Allele Identifier: CA3711908

Gene: HLA-B

Linked Data

• dbSNP Id: rs771028948
• ExAC: 6:31324743 G / GCA
• gnomAD v2: 6-31324743-G-GCA
• gnomAD v3: 6-31356966-G-GCA
• gnomAD v4: 6-31356966-G-GCA
• MyVariant Identifiers: chr6:g.31324743_31324744insCA (hg19) ; chr6:g.31356966_31356967insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356966_31356967insCA , CM000668.2:g.31356966_31356967insCA	GRCh38
NC_000006.11:g.31324743_31324744insCA , CM000668.1:g.31324743_31324744insCA	GRCh37
NC_000006.10:g.31432722_31432723insCA	NCBI36
NG_023187.1:g.5246_5247insTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1547-10_1547-9insTG
ENST00000481849.6:n.1547-10_1547-9insTG
ENST00000497377.6:n.1547-10_1547-9insTG
ENST00000640094.2:c.74-10_74-9insTG	ENSP00000491275.2:n.74-10_74-9insTG
ENST00000696558.1:c.74-10_74-9insTG	ENSP00000512716.1:n.74-10_74-9insTG
ENST00000696559.1:c.74-10_74-9insTG	ENSP00000512717.1:n.74-10_74-9insTG
ENST00000696560.1:c.74-10_74-9insTG	ENSP00000512718.1:n.74-10_74-9insTG
ENST00000696561.1:c.74-10_74-9insTG	ENSP00000512719.1:n.74-10_74-9insTG
ENST00000696562.1:c.74-10_74-9insTG	ENSP00000512720.1:n.74-10_74-9insTG
ENST00000412585.7:c.74-10_74-9insTG MANE Select	ENSP00000399168.2:n.74-10_74-9insTG
ENST00000412585.6:c.74-10_74-9insTG	ENSP00000399168.2:n.74-10_74-9insTG
ENST00000434333.1:c.97_98insTG	ENSP00000405931.1:p.Ser33LeufsTer9
ENST00000498007.1:n.95-10_95-9insTG
ENST00000603274.1:n.320_321insCA
NM_005514.6:c.74-10_74-9insTG	NP_005505.2:n.74-10_74-9insTG
XM_011514556.1:c.97_98insTG	XP_011512858.1:p.Ser33LeufsTer9
XM_011514557.1:c.74-10_74-9insTG	XP_011512859.1:n.74-10_74-9insTG
XR_926175.1:n.84-10_84-9insTG
NM_005514.7:c.74-10_74-9insTG	NP_005505.2:n.74-10_74-9insTG
NM_005514.8:c.74-10_74-9insTG MANE Select	NP_005505.2:n.74-10_74-9insTG