Canonical Allele Identifier: CA566689156

Gene: HLA-B

Linked Data

• gnomAD v2: 6-31324195-T-TAA
• MyVariant Identifiers: chr6:g.31324195_31324196insAA (hg19) ; chr6:g.31356418_31356419insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356419_31356420insAA , CM000668.2:g.31356419_31356420insAA	GRCh38
NC_000006.11:g.31324196_31324197insAA , CM000668.1:g.31324196_31324197insAA	GRCh37
NC_000006.10:g.31432175_31432176insAA	NCBI36
NG_023187.1:g.5794_5795insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1840_1841insTT
ENST00000481849.6:n.1840_1841insTT
ENST00000497377.6:n.1840_1841insTT
ENST00000640094.2:c.367_368insTT	ENSP00000491275.2:p.Tyr123PhefsTer29
ENST00000696558.1:c.367_368insTT	ENSP00000512716.1:p.Tyr123PhefsTer29
ENST00000696559.1:c.367_368insTT	ENSP00000512717.1:p.Tyr123PhefsTer29
ENST00000696560.1:c.367_368insTT	ENSP00000512718.1:p.Tyr123PhefsTer29
ENST00000696561.1:c.367_368insTT	ENSP00000512719.1:p.Tyr123PhefsTer29
ENST00000696562.1:c.367_368insTT	ENSP00000512720.1:p.Tyr123PhefsTer29
ENST00000412585.7:c.367_368insTT MANE Select	ENSP00000399168.2:p.Tyr123PhefsTer29
ENST00000412585.6:c.367_368insTT	ENSP00000399168.2:p.Tyr123PhefsTer29
ENST00000434333.1:c.400_401insTT	ENSP00000405931.1:p.Tyr134PhefsTer29
ENST00000474381.1:n.242_243insTT
ENST00000498007.1:n.633_634insTT
NM_005514.6:c.367_368insTT	NP_005505.2:p.Tyr123PhefsTer29
XM_011514556.1:c.400_401insTT	XP_011512858.1:p.Tyr134PhefsTer29
XM_011514557.1:c.367_368insTT	XP_011512859.1:p.Tyr123PhefsTer29
XR_926175.1:n.377_378insTT
NM_005514.7:c.367_368insTT	NP_005505.2:p.Tyr123PhefsTer29
NM_005514.8:c.367_368insTT MANE Select	NP_005505.2:p.Tyr123PhefsTer29