Canonical Allele Identifier: CA1087467388

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356184-T-TCG
• gnomAD v4: 6-31356184-T-TCG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356185_31356186insGC , CM000668.2:g.31356185_31356186insGC	GRCh38
NC_000006.11:g.31323962_31323963insGC , CM000668.1:g.31323962_31323963insGC	GRCh37
NC_000006.10:g.31431941_31431942insGC	NCBI36
NG_023187.1:g.6028_6029insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2074_2075insCG
ENST00000481849.6:n.2074_2075insCG
ENST00000497377.6:n.2074_2075insCG
ENST00000640094.2:c.601_602insCG	ENSP00000491275.2:p.Asp201AlafsTer14
ENST00000696558.1:c.601_602insCG	ENSP00000512716.1:p.Asp201AlafsTer?
ENST00000696559.1:c.601_602insCG	ENSP00000512717.1:p.Asp201AlafsTer14
ENST00000696560.1:c.601_602insCG	ENSP00000512718.1:p.Asp201AlafsTer14
ENST00000696561.1:c.601_602insCG	ENSP00000512719.1:p.Asp201AlafsTer14
ENST00000696562.1:c.601_602insCG	ENSP00000512720.1:p.Asp201AlafsTer14
ENST00000412585.7:c.601_602insCG MANE Select	ENSP00000399168.2:p.Asp201AlafsTer14
ENST00000412585.6:c.601_602insCG	ENSP00000399168.2:p.Asp201AlafsTer14
ENST00000434333.1:c.634_635insCG	ENSP00000405931.1:p.Asp212AlafsTer14
ENST00000474381.1:n.476_477insCG
ENST00000498007.1:n.867_868insCG
NM_005514.6:c.601_602insCG	NP_005505.2:p.Asp201AlafsTer14
XM_011514556.1:c.634_635insCG	XP_011512858.1:p.Asp212AlafsTer14
XM_011514557.1:c.601_602insCG	XP_011512859.1:p.Asp201AlafsTer14
XR_926175.1:n.611_612insCG
NM_005514.7:c.601_602insCG	NP_005505.2:p.Asp201AlafsTer14
NM_005514.8:c.601_602insCG MANE Select	NP_005505.2:p.Asp201AlafsTer14