Canonical Allele Identifier: CA3711177

Gene: HLA-B

Linked Data

• dbSNP Id: rs554638563
• ExAC: 6:31322277 C / T
• gnomAD v2: 6-31322277-C-T
• gnomAD v3: 6-31354500-C-T
• gnomAD v4: 6-31354500-C-T
• MyVariant Identifiers: chr6:g.31322277C>T (hg19) ; chr6:g.31354500C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354500C>T , CM000668.2:g.31354500C>T	GRCh38
NC_000006.11:g.31322277C>T , CM000668.1:g.31322277C>T	GRCh37
NC_000006.10:g.31430256C>T	NCBI36
NG_023187.1:g.7713G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3119G>A
ENST00000481849.6:n.3079G>A
ENST00000497377.6:n.2986G>A
ENST00000640094.2:c.955G>A	ENSP00000491275.2:p.Val319Met
ENST00000696558.1:c.1141G>A	ENSP00000512716.1:n.1141G>A
ENST00000696559.1:c.1072G>A	ENSP00000512717.1:p.Val358Met
ENST00000696560.1:c.1072G>A	ENSP00000512718.1:p.Val358Met
ENST00000696561.1:c.1072G>A	ENSP00000512719.1:p.Val358Met
ENST00000696562.1:c.1072G>A	ENSP00000512720.1:p.Val358Met
ENST00000412585.7:c.1072G>A MANE Select	ENSP00000399168.2:p.Val358Met
ENST00000412585.6:c.1072G>A	ENSP00000399168.2:p.Val358Met
ENST00000481849.5:n.307G>A
ENST00000497377.5:n.471G>A
NM_005514.6:c.1072G>A	NP_005505.2:p.Val358Met
XM_011514556.1:c.1105G>A	XP_011512858.1:p.Val369Met
XM_011514557.1:c.955G>A	XP_011512859.1:p.Val319Met
XR_926175.1:n.1511G>A
NM_005514.7:c.1072G>A	NP_005505.2:p.Val358Met
NM_005514.8:c.1072G>A MANE Select	NP_005505.2:p.Val358Met