Canonical Allele Identifier: CA2677957742

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356808-A-ATGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356808_31356809insTGG , CM000668.2:g.31356808_31356809insTGG	GRCh38
NC_000006.11:g.31324585_31324586insTGG , CM000668.1:g.31324585_31324586insTGG	GRCh37
NC_000006.10:g.31432564_31432565insTGG	NCBI36
NG_023187.1:g.5404_5405insCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1695_1696insCCA
ENST00000481849.6:n.1695_1696insCCA
ENST00000497377.6:n.1695_1696insCCA
ENST00000640094.2:c.222_223insCCA	ENSP00000491275.2:p.Pro74_Trp75insPro
ENST00000696558.1:c.222_223insCCA	ENSP00000512716.1:p.Pro74_Trp75insPro
ENST00000696559.1:c.222_223insCCA	ENSP00000512717.1:p.Pro74_Trp75insPro
ENST00000696560.1:c.222_223insCCA	ENSP00000512718.1:p.Pro74_Trp75insPro
ENST00000696561.1:c.222_223insCCA	ENSP00000512719.1:p.Pro74_Trp75insPro
ENST00000696562.1:c.222_223insCCA	ENSP00000512720.1:p.Pro74_Trp75insPro
ENST00000412585.7:c.222_223insCCA MANE Select	ENSP00000399168.2:p.Pro74_Trp75insPro
ENST00000412585.6:c.222_223insCCA	ENSP00000399168.2:p.Pro74_Trp75insPro
ENST00000434333.1:c.255_256insCCA	ENSP00000405931.1:p.Pro85_Trp86insPro
ENST00000474381.1:n.97_98insCCA
ENST00000498007.1:n.243_244insCCA
ENST00000603274.1:n.162_163insTGG
NM_005514.6:c.222_223insCCA	NP_005505.2:p.Pro74_Trp75insPro
XM_011514556.1:c.255_256insCCA	XP_011512858.1:p.Pro85_Trp86insPro
XM_011514557.1:c.222_223insCCA	XP_011512859.1:p.Pro74_Trp75insPro
XR_926175.1:n.232_233insCCA
NM_005514.7:c.222_223insCCA	NP_005505.2:p.Pro74_Trp75insPro
NM_005514.8:c.222_223insCCA MANE Select	NP_005505.2:p.Pro74_Trp75insPro