Canonical Allele Identifier: CA2677957645

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356725-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356725_31356726insGG , CM000668.2:g.31356725_31356726insGG	GRCh38
NC_000006.11:g.31324502_31324503insGG , CM000668.1:g.31324502_31324503insGG	GRCh37
NC_000006.10:g.31432481_31432482insGG	NCBI36
NG_023187.1:g.5487_5488insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1778_1779insCC
ENST00000481849.6:n.1778_1779insCC
ENST00000497377.6:n.1778_1779insCC
ENST00000640094.2:c.305_306insCC	ENSP00000491275.2:p.Asn104GlyfsTer?
ENST00000696558.1:c.305_306insCC	ENSP00000512716.1:p.Asn104GlyfsTer?
ENST00000696559.1:c.305_306insCC	ENSP00000512717.1:p.Asn104GlyfsTer?
ENST00000696560.1:c.305_306insCC	ENSP00000512718.1:p.Asn104GlyfsTer?
ENST00000696561.1:c.305_306insCC	ENSP00000512719.1:p.Asn104GlyfsTer?
ENST00000696562.1:c.305_306insCC	ENSP00000512720.1:p.Asn104GlyfsTer?
ENST00000412585.7:c.305_306insCC MANE Select	ENSP00000399168.2:p.Asn104GlyfsTer?
ENST00000412585.6:c.305_306insCC	ENSP00000399168.2:p.Asn104GlyfsTer?
ENST00000434333.1:c.338_339insCC	ENSP00000405931.1:p.Asn115GlyfsTer?
ENST00000474381.1:n.180_181insCC
ENST00000498007.1:n.326_327insCC
ENST00000603274.1:n.79_80insGG
NM_005514.6:c.305_306insCC	NP_005505.2:p.Asn104GlyfsTer?
XM_011514556.1:c.338_339insCC	XP_011512858.1:p.Asn115GlyfsTer?
XM_011514557.1:c.305_306insCC	XP_011512859.1:p.Asn104GlyfsTer?
XR_926175.1:n.315_316insCC
NM_005514.7:c.305_306insCC	NP_005505.2:p.Asn104GlyfsTer?
NM_005514.8:c.305_306insCC MANE Select	NP_005505.2:p.Asn104GlyfsTer?