Canonical Allele Identifier: CA136836133

Gene: HLA-B

Linked Data

• dbSNP Id: rs781665276
• gnomAD v4: 6-31356429-G-GCA
• MyVariant Identifiers: chr6:g.31324206_31324207insCA (hg19) ; chr6:g.31356429_31356430insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356429_31356430insCA , CM000668.2:g.31356429_31356430insCA	GRCh38
NC_000006.11:g.31324206_31324207insCA , CM000668.1:g.31324206_31324207insCA	GRCh37
NC_000006.10:g.31432185_31432186insCA	NCBI36
NG_023187.1:g.5783_5784insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1829_1830insTG
ENST00000481849.6:n.1829_1830insTG
ENST00000497377.6:n.1829_1830insTG
ENST00000640094.2:c.356_357insTG	ENSP00000491275.2:p.Gln120AlafsTer?
ENST00000696558.1:c.356_357insTG	ENSP00000512716.1:p.Gln120AlafsTer?
ENST00000696559.1:c.356_357insTG	ENSP00000512717.1:p.Gln120AlafsTer?
ENST00000696560.1:c.356_357insTG	ENSP00000512718.1:p.Gln120AlafsTer?
ENST00000696561.1:c.356_357insTG	ENSP00000512719.1:p.Gln120AlafsTer?
ENST00000696562.1:c.356_357insTG	ENSP00000512720.1:p.Gln120AlafsTer?
ENST00000412585.7:c.356_357insTG MANE Select	ENSP00000399168.2:p.Gln120AlafsTer?
ENST00000412585.6:c.356_357insTG	ENSP00000399168.2:p.Gln120AlafsTer?
ENST00000434333.1:c.389_390insTG	ENSP00000405931.1:p.Gln131AlafsTer?
ENST00000474381.1:n.231_232insTG
ENST00000498007.1:n.622_623insTG
NM_005514.6:c.356_357insTG	NP_005505.2:p.Gln120AlafsTer?
XM_011514556.1:c.389_390insTG	XP_011512858.1:p.Gln131AlafsTer?
XM_011514557.1:c.356_357insTG	XP_011512859.1:p.Gln120AlafsTer?
XR_926175.1:n.366_367insTG
NM_005514.7:c.356_357insTG	NP_005505.2:p.Gln120AlafsTer?
NM_005514.8:c.356_357insTG MANE Select	NP_005505.2:p.Gln120AlafsTer?