Canonical Allele Identifier: CA2677954703

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355013-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355013_31355014insGG , CM000668.2:g.31355013_31355014insGG	GRCh38
NC_000006.11:g.31322790_31322791insGG , CM000668.1:g.31322790_31322791insGG	GRCh37
NC_000006.10:g.31430769_31430770insGG	NCBI36
NG_023187.1:g.7199_7200insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+93_3059+94insCC
ENST00000481849.6:n.2671_2672insCC
ENST00000497377.6:n.2578_2579insCC
ENST00000640094.2:c.895+303_895+304insCC	ENSP00000491275.2:n.895+303_895+304insCC
ENST00000696558.1:c.1081+93_1081+94insCC	ENSP00000512716.1:n.1081+93_1081+94insCC
ENST00000696559.1:c.1012+93_1012+94insCC	ENSP00000512717.1:n.1012+93_1012+94insCC
ENST00000696560.1:c.1012+93_1012+94insCC	ENSP00000512718.1:n.1012+93_1012+94insCC
ENST00000696561.1:c.1012+93_1012+94insCC	ENSP00000512719.1:n.1012+93_1012+94insCC
ENST00000696562.1:c.1012+93_1012+94insCC	ENSP00000512720.1:n.1012+93_1012+94insCC
ENST00000412585.7:c.1012+93_1012+94insCC MANE Select	ENSP00000399168.2:n.1012+93_1012+94insCC
ENST00000640094.1:c.88+303_88+304insCC	ENSP00000491275.1:n.88+303_88+304insCC
ENST00000412585.6:c.1012+93_1012+94insCC	ENSP00000399168.2:n.1012+93_1012+94insCC
ENST00000497377.5:n.63_64insCC
NM_005514.6:c.1012+93_1012+94insCC	NP_005505.2:n.1012+93_1012+94insCC
XM_011514556.1:c.1045+93_1045+94insCC	XP_011512858.1:n.1045+93_1045+94insCC
XM_011514557.1:c.895+303_895+304insCC	XP_011512859.1:n.895+303_895+304insCC
XR_926175.1:n.1451+93_1451+94insCC
NM_005514.7:c.1012+93_1012+94insCC	NP_005505.2:n.1012+93_1012+94insCC
NM_005514.8:c.1012+93_1012+94insCC MANE Select	NP_005505.2:n.1012+93_1012+94insCC