Canonical Allele Identifier: CA566689385

Gene: HLA-B

Linked Data

• gnomAD v2: 6-31324852-C-CA
• gnomAD v4: 6-31357075-C-CA
• MyVariant Identifiers: chr6:g.31324852_31324853insA (hg19) ; chr6:g.31357075_31357076insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357075_31357076insA , CM000668.2:g.31357075_31357076insA	GRCh38
NC_000006.11:g.31324852_31324853insA , CM000668.1:g.31324852_31324853insA	GRCh37
NC_000006.10:g.31432831_31432832insA	NCBI36
NG_023187.1:g.5137_5138insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1546+10_1546+11insT
ENST00000481849.6:n.1546+10_1546+11insT
ENST00000497377.6:n.1546+10_1546+11insT
ENST00000640094.2:c.73+10_73+11insT	ENSP00000491275.2:n.73+10_73+11insT
ENST00000696558.1:c.73+10_73+11insT	ENSP00000512716.1:n.73+10_73+11insT
ENST00000696559.1:c.73+10_73+11insT	ENSP00000512717.1:n.73+10_73+11insT
ENST00000696560.1:c.73+10_73+11insT	ENSP00000512718.1:n.73+10_73+11insT
ENST00000696561.1:c.73+10_73+11insT	ENSP00000512719.1:n.73+10_73+11insT
ENST00000696562.1:c.73+10_73+11insT	ENSP00000512720.1:n.73+10_73+11insT
ENST00000412585.7:c.73+10_73+11insT MANE Select	ENSP00000399168.2:n.73+10_73+11insT
ENST00000412585.6:c.73+10_73+11insT	ENSP00000399168.2:n.73+10_73+11insT
ENST00000434333.1:c.-13_-12insT	ENSP00000405931.1:n.-13_-12insT
ENST00000498007.1:n.94+10_94+11insT
ENST00000603274.1:n.429_430insA
NM_005514.6:c.73+10_73+11insT	NP_005505.2:n.73+10_73+11insT
XM_011514556.1:c.-13_-12insT	XP_011512858.1:n.-13_-12insT
XM_011514557.1:c.73+10_73+11insT	XP_011512859.1:n.73+10_73+11insT
XR_926175.1:n.83+10_83+11insT
NM_005514.7:c.73+10_73+11insT	NP_005505.2:n.73+10_73+11insT
NM_005514.8:c.73+10_73+11insT MANE Select	NP_005505.2:n.73+10_73+11insT