Canonical Allele Identifier: CA1087444818

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31357055-A-ACC
• gnomAD v4: 6-31357055-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357055_31357056insCC , CM000668.2:g.31357055_31357056insCC	GRCh38
NC_000006.11:g.31324832_31324833insCC , CM000668.1:g.31324832_31324833insCC	GRCh37
NC_000006.10:g.31432811_31432812insCC	NCBI36
NG_023187.1:g.5157_5158insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1546+30_1546+31insGG
ENST00000481849.6:n.1546+30_1546+31insGG
ENST00000497377.6:n.1546+30_1546+31insGG
ENST00000640094.2:c.73+30_73+31insGG	ENSP00000491275.2:n.73+30_73+31insGG
ENST00000696558.1:c.73+30_73+31insGG	ENSP00000512716.1:n.73+30_73+31insGG
ENST00000696559.1:c.73+30_73+31insGG	ENSP00000512717.1:n.73+30_73+31insGG
ENST00000696560.1:c.73+30_73+31insGG	ENSP00000512718.1:n.73+30_73+31insGG
ENST00000696561.1:c.73+30_73+31insGG	ENSP00000512719.1:n.73+30_73+31insGG
ENST00000696562.1:c.73+30_73+31insGG	ENSP00000512720.1:n.73+30_73+31insGG
ENST00000412585.7:c.73+30_73+31insGG MANE Select	ENSP00000399168.2:n.73+30_73+31insGG
ENST00000412585.6:c.73+30_73+31insGG	ENSP00000399168.2:n.73+30_73+31insGG
ENST00000434333.1:c.8_9insGG	ENSP00000405931.1:p.Ala4ValfsTer?
ENST00000498007.1:n.94+30_94+31insGG
ENST00000603274.1:n.409_410insCC
NM_005514.6:c.73+30_73+31insGG	NP_005505.2:n.73+30_73+31insGG
XM_011514556.1:c.8_9insGG	XP_011512858.1:p.Ala4ValfsTer?
XM_011514557.1:c.73+30_73+31insGG	XP_011512859.1:n.73+30_73+31insGG
XR_926175.1:n.83+30_83+31insGG
NM_005514.7:c.73+30_73+31insGG	NP_005505.2:n.73+30_73+31insGG
NM_005514.8:c.73+30_73+31insGG MANE Select	NP_005505.2:n.73+30_73+31insGG