Canonical Allele Identifier: CA449599570

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354495-A-G
• MyVariant Identifiers: chr6:g.31322272A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354495A>G , CM000668.2:g.31354495A>G	GRCh38
NC_000006.11:g.31322272A>G , CM000668.1:g.31322272A>G	GRCh37
NC_000006.10:g.31430251A>G	NCBI36
NG_023187.1:g.7718T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3124T>C
ENST00000481849.6:n.3084T>C
ENST00000497377.6:n.2991T>C
ENST00000640094.2:c.960T>C	ENSP00000491275.2:p.Ser320=
ENST00000696558.1:c.1146T>C	ENSP00000512716.1:n.1146T>C
ENST00000696559.1:c.1077T>C	ENSP00000512717.1:p.Ser359=
ENST00000696560.1:c.1077T>C	ENSP00000512718.1:p.Ser359=
ENST00000696561.1:c.1077T>C	ENSP00000512719.1:p.Ser359=
ENST00000696562.1:c.1077T>C	ENSP00000512720.1:p.Ser359=
ENST00000412585.7:c.1077T>C MANE Select	ENSP00000399168.2:p.Ser359=
ENST00000412585.6:c.1077T>C	ENSP00000399168.2:p.Ser359=
ENST00000481849.5:n.312T>C
ENST00000497377.5:n.476T>C
NM_005514.6:c.1077T>C	NP_005505.2:p.Ser359=
XM_011514556.1:c.1110T>C	XP_011512858.1:p.Ser370=
XM_011514557.1:c.960T>C	XP_011512859.1:p.Ser320=
XR_926175.1:n.1516T>C
NM_005514.7:c.1077T>C	NP_005505.2:p.Ser359=
NM_005514.8:c.1077T>C MANE Select	NP_005505.2:p.Ser359=