Canonical Allele Identifier: CA2677953043

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354113-T-TGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354114_31354115insTGG , CM000668.2:g.31354114_31354115insTGG	GRCh38
NC_000006.11:g.31321891_31321892insTGG , CM000668.1:g.31321891_31321892insTGG	GRCh37
NC_000006.10:g.31429870_31429871insTGG	NCBI36
NG_023187.1:g.8099_8100insCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3323_3324insCAC
ENST00000481849.6:n.3283_3284insCAC
ENST00000497377.6:n.3190_3191insCAC
ENST00000696558.1:c.1345_1346insCAC	ENSP00000512716.1:n.1345_1346insCAC
ENST00000696559.1:c.*187_*188insCAC	ENSP00000512717.1:n.*187_*188insCAC
ENST00000696560.1:c.*187_*188insCAC	ENSP00000512718.1:n.*187_*188insCAC
ENST00000696561.1:c.*187_*188insCAC	ENSP00000512719.1:n.*187_*188insCAC
ENST00000696562.1:c.*187_*188insCAC	ENSP00000512720.1:n.*187_*188insCAC
ENST00000412585.7:c.*187_*188insCAC MANE Select	ENSP00000399168.2:n.*187_*188insCAC
ENST00000412585.6:c.*187_*188insCAC	ENSP00000399168.2:n.*187_*188insCAC
ENST00000481849.5:n.511_512insCAC
ENST00000497377.5:n.675_676insCAC
NM_005514.6:c.*187_*188insCAC	NP_005505.2:n.*187_*188insCAC
XM_011514556.1:c.*187_*188insCAC	XP_011512858.1:n.*187_*188insCAC
XM_011514557.1:c.*187_*188insCAC	XP_011512859.1:n.*187_*188insCAC
XR_926175.1:n.1715_1716insCAC
NM_005514.7:c.*187_*188insCAC	NP_005505.2:n.*187_*188insCAC
NM_005514.8:c.*187_*188insCAC MANE Select	NP_005505.2:n.*187_*188insCAC