Canonical Allele Identifier: CA2677956569

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356185-C-CTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356185_31356186insTA , CM000668.2:g.31356185_31356186insTA	GRCh38
NC_000006.11:g.31323962_31323963insTA , CM000668.1:g.31323962_31323963insTA	GRCh37
NC_000006.10:g.31431941_31431942insTA	NCBI36
NG_023187.1:g.6027_6028insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2073_2074insTA
ENST00000481849.6:n.2073_2074insTA
ENST00000497377.6:n.2073_2074insTA
ENST00000640094.2:c.600_601insTA	ENSP00000491275.2:p.Asp201Ter
ENST00000696558.1:c.600_601insTA	ENSP00000512716.1:p.Asp201Ter
ENST00000696559.1:c.600_601insTA	ENSP00000512717.1:p.Asp201Ter
ENST00000696560.1:c.600_601insTA	ENSP00000512718.1:p.Asp201Ter
ENST00000696561.1:c.600_601insTA	ENSP00000512719.1:p.Asp201Ter
ENST00000696562.1:c.600_601insTA	ENSP00000512720.1:p.Asp201Ter
ENST00000412585.7:c.600_601insTA MANE Select	ENSP00000399168.2:p.Asp201Ter
ENST00000412585.6:c.600_601insTA	ENSP00000399168.2:p.Asp201Ter
ENST00000434333.1:c.633_634insTA	ENSP00000405931.1:p.Asp212Ter
ENST00000474381.1:n.475_476insTA
ENST00000498007.1:n.866_867insTA
NM_005514.6:c.600_601insTA	NP_005505.2:p.Asp201Ter
XM_011514556.1:c.633_634insTA	XP_011512858.1:p.Asp212Ter
XM_011514557.1:c.600_601insTA	XP_011512859.1:p.Asp201Ter
XR_926175.1:n.610_611insTA
NM_005514.7:c.600_601insTA	NP_005505.2:p.Asp201Ter
NM_005514.8:c.600_601insTA MANE Select	NP_005505.2:p.Asp201Ter