Canonical Allele Identifier: CA566689265

Gene: HLA-B

Linked Data

• gnomAD v2: 6-31323960-G-GCTGCAGCGTC
• MyVariant Identifiers: chr6:g.31323960_31323961insCTGCAGCGTC (hg19) ; chr6:g.31356183_31356184insCTGCAGCGTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356183_31356184insCTGCAGCGTC , CM000668.2:g.31356183_31356184insCTGCAGCGTC	GRCh38
NC_000006.11:g.31323960_31323961insCTGCAGCGTC , CM000668.1:g.31323960_31323961insCTGCAGCGTC	GRCh37
NC_000006.10:g.31431939_31431940insCTGCAGCGTC	NCBI36
NG_023187.1:g.6029_6030insGACGCTGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2075_2076insGACGCTGCAG
ENST00000481849.6:n.2075_2076insGACGCTGCAG
ENST00000497377.6:n.2075_2076insGACGCTGCAG
ENST00000640094.2:c.602_603insGACGCTGCAG	ENSP00000491275.2:p.Asp201GlufsTer10
ENST00000696558.1:c.602_603insGACGCTGCAG	ENSP00000512716.1:p.Asp201GlufsTer10
ENST00000696559.1:c.602_603insGACGCTGCAG	ENSP00000512717.1:p.Asp201GlufsTer10
ENST00000696560.1:c.602_603insGACGCTGCAG	ENSP00000512718.1:p.Asp201GlufsTer10
ENST00000696561.1:c.602_603insGACGCTGCAG	ENSP00000512719.1:p.Asp201GlufsTer10
ENST00000696562.1:c.602_603insGACGCTGCAG	ENSP00000512720.1:p.Asp201GlufsTer10
ENST00000412585.7:c.602_603insGACGCTGCAG MANE Select	ENSP00000399168.2:p.Asp201GlufsTer10
ENST00000412585.6:c.602_603insGACGCTGCAG	ENSP00000399168.2:p.Asp201GlufsTer10
ENST00000434333.1:c.635_636insGACGCTGCAG	ENSP00000405931.1:p.Asp212GlufsTer10
ENST00000474381.1:n.477_478insGACGCTGCAG
ENST00000498007.1:n.868_869insGACGCTGCAG
NM_005514.6:c.602_603insGACGCTGCAG	NP_005505.2:p.Asp201GlufsTer10
XM_011514556.1:c.635_636insGACGCTGCAG	XP_011512858.1:p.Asp212GlufsTer10
XM_011514557.1:c.602_603insGACGCTGCAG	XP_011512859.1:p.Asp201GlufsTer10
XR_926175.1:n.612_613insGACGCTGCAG
NM_005514.7:c.602_603insGACGCTGCAG	NP_005505.2:p.Asp201GlufsTer10
NM_005514.8:c.602_603insGACGCTGCAG MANE Select	NP_005505.2:p.Asp201GlufsTer10