Canonical Allele Identifier: CA2677957658

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356734-TCG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356735_31356736del , CM000668.2:g.31356735_31356736del	GRCh38
NC_000006.11:g.31324512_31324513del , CM000668.1:g.31324512_31324513del	GRCh37
NC_000006.10:g.31432491_31432492del	NCBI36
NG_023187.1:g.5477_5478del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1768_1769del
ENST00000481849.6:n.1768_1769del
ENST00000497377.6:n.1768_1769del
ENST00000640094.2:c.295_296del	ENSP00000491275.2:p.Ser101ProfsTer?
ENST00000696558.1:c.295_296del	ENSP00000512716.1:p.Ser101ProfsTer?
ENST00000696559.1:c.295_296del	ENSP00000512717.1:p.Ser101ProfsTer?
ENST00000696560.1:c.295_296del	ENSP00000512718.1:p.Ser101ProfsTer?
ENST00000696561.1:c.295_296del	ENSP00000512719.1:p.Ser101ProfsTer?
ENST00000696562.1:c.295_296del	ENSP00000512720.1:p.Ser101ProfsTer?
ENST00000412585.7:c.295_296del MANE Select	ENSP00000399168.2:p.Ser101ProfsTer?
ENST00000412585.6:c.295_296del	ENSP00000399168.2:p.Ser101ProfsTer?
ENST00000434333.1:c.328_329del	ENSP00000405931.1:p.Ser112ProfsTer?
ENST00000474381.1:n.170_171del
ENST00000498007.1:n.316_317del
ENST00000603274.1:n.89_90del
NM_005514.6:c.295_296del	NP_005505.2:p.Ser101ProfsTer?
XM_011514556.1:c.328_329del	XP_011512858.1:p.Ser112ProfsTer?
XM_011514557.1:c.295_296del	XP_011512859.1:p.Ser101ProfsTer?
XR_926175.1:n.305_306del
NM_005514.7:c.295_296del	NP_005505.2:p.Ser101ProfsTer?
NM_005514.8:c.295_296del MANE Select	NP_005505.2:p.Ser101ProfsTer?