Canonical Allele Identifier: CA566689381

Gene: HLA-B

Linked Data

• gnomAD v2: 6-31324831-C-CAT
• gnomAD v4: 6-31357054-C-CAT
• MyVariant Identifiers: chr6:g.31324831_31324832insAT (hg19) ; chr6:g.31357054_31357055insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357055_31357056insTA , CM000668.2:g.31357055_31357056insTA	GRCh38
NC_000006.11:g.31324832_31324833insTA , CM000668.1:g.31324832_31324833insTA	GRCh37
NC_000006.10:g.31432811_31432812insTA	NCBI36
NG_023187.1:g.5158_5159insAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1546+31_1546+32insAT
ENST00000481849.6:n.1546+31_1546+32insAT
ENST00000497377.6:n.1546+31_1546+32insAT
ENST00000640094.2:c.73+31_73+32insAT	ENSP00000491275.2:n.73+31_73+32insAT
ENST00000696558.1:c.73+31_73+32insAT	ENSP00000512716.1:n.73+31_73+32insAT
ENST00000696559.1:c.73+31_73+32insAT	ENSP00000512717.1:n.73+31_73+32insAT
ENST00000696560.1:c.73+31_73+32insAT	ENSP00000512718.1:n.73+31_73+32insAT
ENST00000696561.1:c.73+31_73+32insAT	ENSP00000512719.1:n.73+31_73+32insAT
ENST00000696562.1:c.73+31_73+32insAT	ENSP00000512720.1:n.73+31_73+32insAT
ENST00000412585.7:c.73+31_73+32insAT MANE Select	ENSP00000399168.2:n.73+31_73+32insAT
ENST00000412585.6:c.73+31_73+32insAT	ENSP00000399168.2:n.73+31_73+32insAT
ENST00000434333.1:c.9_10insAT	ENSP00000405931.1:p.Ala4MetfsTer?
ENST00000498007.1:n.94+31_94+32insAT
ENST00000603274.1:n.409_410insTA
NM_005514.6:c.73+31_73+32insAT	NP_005505.2:n.73+31_73+32insAT
XM_011514556.1:c.9_10insAT	XP_011512858.1:p.Ala4MetfsTer?
XM_011514557.1:c.73+31_73+32insAT	XP_011512859.1:n.73+31_73+32insAT
XR_926175.1:n.83+31_83+32insAT
NM_005514.7:c.73+31_73+32insAT	NP_005505.2:n.73+31_73+32insAT
NM_005514.8:c.73+31_73+32insAT MANE Select	NP_005505.2:n.73+31_73+32insAT