Canonical Allele Identifier: CA3711531

Gene: HLA-B

Linked Data

• dbSNP Id: rs760644662
• ExAC: 6:31324021 C / CTG
• gnomAD v2: 6-31324021-C-CTG
• gnomAD v3: 6-31356244-C-CTG
• gnomAD v4: 6-31356244-C-CTG
• MyVariant Identifiers: chr6:g.31324021_31324022insTG (hg19) ; chr6:g.31356244_31356245insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356245_31356246insGT , CM000668.2:g.31356245_31356246insGT	GRCh38
NC_000006.11:g.31324022_31324023insGT , CM000668.1:g.31324022_31324023insGT	GRCh37
NC_000006.10:g.31432001_31432002insGT	NCBI36
NG_023187.1:g.5968_5969insCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2014_2015insCA
ENST00000481849.6:n.2014_2015insCA
ENST00000497377.6:n.2014_2015insCA
ENST00000640094.2:c.541_542insCA	ENSP00000491275.2:p.Arg181ThrfsTer?
ENST00000696558.1:c.541_542insCA	ENSP00000512716.1:p.Arg181ThrfsTer?
ENST00000696559.1:c.541_542insCA	ENSP00000512717.1:p.Arg181ThrfsTer?
ENST00000696560.1:c.541_542insCA	ENSP00000512718.1:p.Arg181ThrfsTer?
ENST00000696561.1:c.541_542insCA	ENSP00000512719.1:p.Arg181ThrfsTer?
ENST00000696562.1:c.541_542insCA	ENSP00000512720.1:p.Arg181ThrfsTer?
ENST00000412585.7:c.541_542insCA MANE Select	ENSP00000399168.2:p.Arg181ThrfsTer?
ENST00000412585.6:c.541_542insCA	ENSP00000399168.2:p.Arg181ThrfsTer?
ENST00000434333.1:c.574_575insCA	ENSP00000405931.1:p.Arg192ThrfsTer?
ENST00000474381.1:n.416_417insCA
ENST00000498007.1:n.807_808insCA
NM_005514.6:c.541_542insCA	NP_005505.2:p.Arg181ThrfsTer?
XM_011514556.1:c.574_575insCA	XP_011512858.1:p.Arg192ThrfsTer?
XM_011514557.1:c.541_542insCA	XP_011512859.1:p.Arg181ThrfsTer?
XR_926175.1:n.551_552insCA
NM_005514.7:c.541_542insCA	NP_005505.2:p.Arg181ThrfsTer?
NM_005514.8:c.541_542insCA MANE Select	NP_005505.2:p.Arg181ThrfsTer?