Canonical Allele Identifier: CA136836097

Gene: HLA-B

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356423_31356424delinsCG , CM000668.2:g.31356423_31356424delinsCG	GRCh38
NC_000006.11:g.31324200_31324201delinsCG , CM000668.1:g.31324200_31324201delinsCG	GRCh37
NC_000006.10:g.31432179_31432180delinsCG	NCBI36
NG_023187.1:g.5789_5790delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1835_1836delinsCG
ENST00000481849.6:n.1835_1836delinsCG
ENST00000497377.6:n.1835_1836delinsCG
ENST00000640094.2:c.362_363delinsCG	ENSP00000491275.2:p.Ser121Thr
ENST00000696558.1:c.362_363delinsCG	ENSP00000512716.1:p.Ser121Thr
ENST00000696559.1:c.362_363delinsCG	ENSP00000512717.1:p.Ser121Thr
ENST00000696560.1:c.362_363delinsCG	ENSP00000512718.1:p.Ser121Thr
ENST00000696561.1:c.362_363delinsCG	ENSP00000512719.1:p.Ser121Thr
ENST00000696562.1:c.362_363delinsCG	ENSP00000512720.1:p.Ser121Thr
ENST00000412585.7:c.362_363delinsCG MANE Select	ENSP00000399168.2:p.Ser121Thr
ENST00000412585.6:c.362_363delinsCG	ENSP00000399168.2:p.Ser121Thr
ENST00000434333.1:c.395_396delinsCG	ENSP00000405931.1:p.Ser132Thr
ENST00000474381.1:n.237_238delinsCG
ENST00000498007.1:n.628_629delinsCG
NM_005514.6:c.362_363delinsCG	NP_005505.2:p.Ser121Thr
XM_011514556.1:c.395_396delinsCG	XP_011512858.1:p.Ser132Thr
XM_011514557.1:c.362_363delinsCG	XP_011512859.1:p.Ser121Thr
XR_926175.1:n.372_373delinsCG
NM_005514.7:c.362_363delinsCG	NP_005505.2:p.Ser121Thr
NM_005514.8:c.362_363delinsCG MANE Select	NP_005505.2:p.Ser121Thr