Canonical Allele Identifier: CA2677957554

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356598-G-GCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356599_31356600insTC , CM000668.2:g.31356599_31356600insTC	GRCh38
NC_000006.11:g.31324376_31324377insTC , CM000668.1:g.31324376_31324377insTC	GRCh37
NC_000006.10:g.31432355_31432356insTC	NCBI36
NG_023187.1:g.5614_5615insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1816+89_1816+90insAG
ENST00000481849.6:n.1816+89_1816+90insAG
ENST00000497377.6:n.1816+89_1816+90insAG
ENST00000640094.2:c.343+89_343+90insAG	ENSP00000491275.2:n.343+89_343+90insAG
ENST00000696558.1:c.343+89_343+90insAG	ENSP00000512716.1:n.343+89_343+90insAG
ENST00000696559.1:c.343+89_343+90insAG	ENSP00000512717.1:n.343+89_343+90insAG
ENST00000696560.1:c.343+89_343+90insAG	ENSP00000512718.1:n.343+89_343+90insAG
ENST00000696561.1:c.343+89_343+90insAG	ENSP00000512719.1:n.343+89_343+90insAG
ENST00000696562.1:c.343+89_343+90insAG	ENSP00000512720.1:n.343+89_343+90insAG
ENST00000412585.7:c.343+89_343+90insAG MANE Select	ENSP00000399168.2:n.343+89_343+90insAG
ENST00000412585.6:c.343+89_343+90insAG	ENSP00000399168.2:n.343+89_343+90insAG
ENST00000434333.1:c.376+89_376+90insAG	ENSP00000405931.1:n.376+89_376+90insAG
ENST00000474381.1:n.218+89_218+90insAG
ENST00000498007.1:n.453_454insAG
NM_005514.6:c.343+89_343+90insAG	NP_005505.2:n.343+89_343+90insAG
XM_011514556.1:c.376+89_376+90insAG	XP_011512858.1:n.376+89_376+90insAG
XM_011514557.1:c.343+89_343+90insAG	XP_011512859.1:n.343+89_343+90insAG
XR_926175.1:n.353+89_353+90insAG
NM_005514.7:c.343+89_343+90insAG	NP_005505.2:n.343+89_343+90insAG
NM_005514.8:c.343+89_343+90insAG MANE Select	NP_005505.2:n.343+89_343+90insAG