Canonical Allele Identifier: CA3711946

Gene: HLA-B

Linked Data

• dbSNP Id: rs761604346
• ExAC: 6:31324831 C / CAA
• gnomAD v2: 6-31324831-C-CAA
• gnomAD v4: 6-31357054-C-CAA
• MyVariant Identifiers: chr6:g.31324831_31324832insAA (hg19) ; chr6:g.31357054_31357055insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357055_31357056insAA , CM000668.2:g.31357055_31357056insAA	GRCh38
NC_000006.11:g.31324832_31324833insAA , CM000668.1:g.31324832_31324833insAA	GRCh37
NC_000006.10:g.31432811_31432812insAA	NCBI36
NG_023187.1:g.5158_5159insTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1546+31_1546+32insTT
ENST00000481849.6:n.1546+31_1546+32insTT
ENST00000497377.6:n.1546+31_1546+32insTT
ENST00000640094.2:c.73+31_73+32insTT	ENSP00000491275.2:n.73+31_73+32insTT
ENST00000696558.1:c.73+31_73+32insTT	ENSP00000512716.1:n.73+31_73+32insTT
ENST00000696559.1:c.73+31_73+32insTT	ENSP00000512717.1:n.73+31_73+32insTT
ENST00000696560.1:c.73+31_73+32insTT	ENSP00000512718.1:n.73+31_73+32insTT
ENST00000696561.1:c.73+31_73+32insTT	ENSP00000512719.1:n.73+31_73+32insTT
ENST00000696562.1:c.73+31_73+32insTT	ENSP00000512720.1:n.73+31_73+32insTT
ENST00000412585.7:c.73+31_73+32insTT MANE Select	ENSP00000399168.2:n.73+31_73+32insTT
ENST00000412585.6:c.73+31_73+32insTT	ENSP00000399168.2:n.73+31_73+32insTT
ENST00000434333.1:c.9_10insTT	ENSP00000405931.1:p.Ala4LeufsTer?
ENST00000498007.1:n.94+31_94+32insTT
ENST00000603274.1:n.409_410insAA
NM_005514.6:c.73+31_73+32insTT	NP_005505.2:n.73+31_73+32insTT
XM_011514556.1:c.9_10insTT	XP_011512858.1:p.Ala4LeufsTer?
XM_011514557.1:c.73+31_73+32insTT	XP_011512859.1:n.73+31_73+32insTT
XR_926175.1:n.83+31_83+32insTT
NM_005514.7:c.73+31_73+32insTT	NP_005505.2:n.73+31_73+32insTT
NM_005514.8:c.73+31_73+32insTT MANE Select	NP_005505.2:n.73+31_73+32insTT