Canonical Allele Identifier: CA1619112863

Gene: HLA-B

Linked Data

• dbSNP Id: rs1767071500

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356717_31356718delinsGC , CM000668.2:g.31356717_31356718delinsGC	GRCh38
NC_000006.11:g.31324494_31324495delinsGC , CM000668.1:g.31324494_31324495delinsGC	GRCh37
NC_000006.10:g.31432473_31432474delinsGC	NCBI36
NG_023187.1:g.5495_5496delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1786_1787delinsGC
ENST00000481849.6:n.1786_1787delinsGC
ENST00000497377.6:n.1786_1787delinsGC
ENST00000640094.2:c.313_314delinsGC	ENSP00000491275.2:p.Leu105Ala
ENST00000696558.1:c.313_314delinsGC	ENSP00000512716.1:p.Leu105Ala
ENST00000696559.1:c.313_314delinsGC	ENSP00000512717.1:p.Leu105Ala
ENST00000696560.1:c.313_314delinsGC	ENSP00000512718.1:p.Leu105Ala
ENST00000696561.1:c.313_314delinsGC	ENSP00000512719.1:p.Leu105Ala
ENST00000696562.1:c.313_314delinsGC	ENSP00000512720.1:p.Leu105Ala
ENST00000412585.7:c.313_314delinsGC MANE Select	ENSP00000399168.2:p.Leu105Ala
ENST00000412585.6:c.313_314delinsGC	ENSP00000399168.2:p.Leu105Ala
ENST00000434333.1:c.346_347delinsGC	ENSP00000405931.1:p.Leu116Ala
ENST00000474381.1:n.188_189delinsGC
ENST00000498007.1:n.334_335delinsGC
ENST00000603274.1:n.71_72delinsGC
NM_005514.6:c.313_314delinsGC	NP_005505.2:p.Leu105Ala
XM_011514556.1:c.346_347delinsGC	XP_011512858.1:p.Leu116Ala
XM_011514557.1:c.313_314delinsGC	XP_011512859.1:p.Leu105Ala
XR_926175.1:n.323_324delinsGC
NM_005514.7:c.313_314delinsGC	NP_005505.2:p.Leu105Ala
NM_005514.8:c.313_314delinsGC MANE Select	NP_005505.2:p.Leu105Ala