Canonical Allele Identifier: CA3711492

Gene: HLA-B

Linked Data

• dbSNP Id: rs766909113
• ExAC: 6:31323960 G / GGC
• gnomAD v3: 6-31356183-G-GGC
• gnomAD v4: 6-31356183-G-GGC
• MyVariant Identifiers: chr6:g.31323960_31323961insGC (hg19) ; chr6:g.31356183_31356184insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356183_31356184insGC , CM000668.2:g.31356183_31356184insGC	GRCh38
NC_000006.11:g.31323960_31323961insGC , CM000668.1:g.31323960_31323961insGC	GRCh37
NC_000006.10:g.31431939_31431940insGC	NCBI36
NG_023187.1:g.6029_6030insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2075_2076insGC
ENST00000481849.6:n.2075_2076insGC
ENST00000497377.6:n.2075_2076insGC
ENST00000640094.2:c.602_603insGC	ENSP00000491275.2:p.Asp201GlufsTer14
ENST00000696558.1:c.602_603insGC	ENSP00000512716.1:p.Asp201GlufsTer?
ENST00000696559.1:c.602_603insGC	ENSP00000512717.1:p.Asp201GlufsTer14
ENST00000696560.1:c.602_603insGC	ENSP00000512718.1:p.Asp201GlufsTer14
ENST00000696561.1:c.602_603insGC	ENSP00000512719.1:p.Asp201GlufsTer14
ENST00000696562.1:c.602_603insGC	ENSP00000512720.1:p.Asp201GlufsTer14
ENST00000412585.7:c.602_603insGC MANE Select	ENSP00000399168.2:p.Asp201GlufsTer14
ENST00000412585.6:c.602_603insGC	ENSP00000399168.2:p.Asp201GlufsTer14
ENST00000434333.1:c.635_636insGC	ENSP00000405931.1:p.Asp212GlufsTer14
ENST00000474381.1:n.477_478insGC
ENST00000498007.1:n.868_869insGC
NM_005514.6:c.602_603insGC	NP_005505.2:p.Asp201GlufsTer14
XM_011514556.1:c.635_636insGC	XP_011512858.1:p.Asp212GlufsTer14
XM_011514557.1:c.602_603insGC	XP_011512859.1:p.Asp201GlufsTer14
XR_926175.1:n.612_613insGC
NM_005514.7:c.602_603insGC	NP_005505.2:p.Asp201GlufsTer14
NM_005514.8:c.602_603insGC MANE Select	NP_005505.2:p.Asp201GlufsTer14