Canonical Allele Identifier: CA1619114146

Gene: HLA-B

Linked Data

• dbSNP Id: rs1767173555
• gnomAD v4: 6-31357069-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357069_31357070insG , CM000668.2:g.31357069_31357070insG	GRCh38
NC_000006.11:g.31324846_31324847insG , CM000668.1:g.31324846_31324847insG	GRCh37
NC_000006.10:g.31432825_31432826insG	NCBI36
NG_023187.1:g.5143_5144insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1546+16_1546+17insC
ENST00000481849.6:n.1546+16_1546+17insC
ENST00000497377.6:n.1546+16_1546+17insC
ENST00000640094.2:c.73+16_73+17insC	ENSP00000491275.2:n.73+16_73+17insC
ENST00000696558.1:c.73+16_73+17insC	ENSP00000512716.1:n.73+16_73+17insC
ENST00000696559.1:c.73+16_73+17insC	ENSP00000512717.1:n.73+16_73+17insC
ENST00000696560.1:c.73+16_73+17insC	ENSP00000512718.1:n.73+16_73+17insC
ENST00000696561.1:c.73+16_73+17insC	ENSP00000512719.1:n.73+16_73+17insC
ENST00000696562.1:c.73+16_73+17insC	ENSP00000512720.1:n.73+16_73+17insC
ENST00000412585.7:c.73+16_73+17insC MANE Select	ENSP00000399168.2:n.73+16_73+17insC
ENST00000412585.6:c.73+16_73+17insC	ENSP00000399168.2:n.73+16_73+17insC
ENST00000434333.1:c.-7_-6insC	ENSP00000405931.1:n.-7_-6insC
ENST00000498007.1:n.94+16_94+17insC
ENST00000603274.1:n.423_424insG
NM_005514.6:c.73+16_73+17insC	NP_005505.2:n.73+16_73+17insC
XM_011514556.1:c.-7_-6insC	XP_011512858.1:n.-7_-6insC
XM_011514557.1:c.73+16_73+17insC	XP_011512859.1:n.73+16_73+17insC
XR_926175.1:n.83+16_83+17insC
NM_005514.7:c.73+16_73+17insC	NP_005505.2:n.73+16_73+17insC
NM_005514.8:c.73+16_73+17insC MANE Select	NP_005505.2:n.73+16_73+17insC