Canonical Allele Identifier: CA2677957740

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356805-TCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356807_31356809del , CM000668.2:g.31356807_31356809del	GRCh38
NC_000006.11:g.31324584_31324586del , CM000668.1:g.31324584_31324586del	GRCh37
NC_000006.10:g.31432563_31432565del	NCBI36
NG_023187.1:g.5405_5407del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1696_1698del
ENST00000481849.6:n.1696_1698del
ENST00000497377.6:n.1696_1698del
ENST00000640094.2:c.223_225del	ENSP00000491275.2:p.Trp75del
ENST00000696558.1:c.223_225del	ENSP00000512716.1:p.Trp75del
ENST00000696559.1:c.223_225del	ENSP00000512717.1:p.Trp75del
ENST00000696560.1:c.223_225del	ENSP00000512718.1:p.Trp75del
ENST00000696561.1:c.223_225del	ENSP00000512719.1:p.Trp75del
ENST00000696562.1:c.223_225del	ENSP00000512720.1:p.Trp75del
ENST00000412585.7:c.223_225del MANE Select	ENSP00000399168.2:p.Trp75del
ENST00000412585.6:c.223_225del	ENSP00000399168.2:p.Trp75del
ENST00000434333.1:c.256_258del	ENSP00000405931.1:p.Trp86del
ENST00000474381.1:n.98_100del
ENST00000498007.1:n.244_246del
ENST00000603274.1:n.161_163del
NM_005514.6:c.223_225del	NP_005505.2:p.Trp75del
XM_011514556.1:c.256_258del	XP_011512858.1:p.Trp86del
XM_011514557.1:c.223_225del	XP_011512859.1:p.Trp75del
XR_926175.1:n.233_235del
NM_005514.7:c.223_225del	NP_005505.2:p.Trp75del
NM_005514.8:c.223_225del MANE Select	NP_005505.2:p.Trp75del