Canonical Allele Identifier: CA3711251

Gene: HLA-B

Linked Data

• dbSNP Id: rs41556216
• ExAC: 6:31322885 T / A
• gnomAD v2: 6-31322885-T-A
• gnomAD v3: 6-31355108-T-A
• gnomAD v4: 6-31355108-T-A
• MyVariant Identifiers: chr6:g.31322885T>A (hg19) ; chr6:g.31355108T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355108T>A , CM000668.2:g.31355108T>A	GRCh38
NC_000006.11:g.31322885T>A , CM000668.1:g.31322885T>A	GRCh37
NC_000006.10:g.31430864T>A	NCBI36
NG_023187.1:g.7105A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3058A>T
ENST00000481849.6:n.2577A>T
ENST00000497377.6:n.2484A>T
ENST00000640094.2:c.895+209A>T	ENSP00000491275.2:n.895+209A>T
ENST00000696558.1:c.1080A>T	ENSP00000512716.1:n.1080A>T
ENST00000696559.1:c.1011A>T	ENSP00000512717.1:p.Ser337=
ENST00000696560.1:c.1011A>T	ENSP00000512718.1:p.Ser337=
ENST00000696561.1:c.1011A>T	ENSP00000512719.1:p.Ser337=
ENST00000696562.1:c.1011A>T	ENSP00000512720.1:p.Ser337=
ENST00000412585.7:c.1011A>T MANE Select	ENSP00000399168.2:p.Ser337=
ENST00000640094.1:c.88+209A>T	ENSP00000491275.1:n.88+209A>T
ENST00000412585.6:c.1011A>T	ENSP00000399168.2:p.Ser337=
NM_005514.6:c.1011A>T	NP_005505.2:p.Ser337=
XM_011514556.1:c.1044A>T	XP_011512858.1:p.Ser348=
XM_011514557.1:c.895+209A>T	XP_011512859.1:n.895+209A>T
XR_926175.1:n.1450A>T
NM_005514.7:c.1011A>T	NP_005505.2:p.Ser337=
NM_005514.8:c.1011A>T MANE Select	NP_005505.2:p.Ser337=