Canonical Allele Identifier: CA363312624

Gene: HLA-B

Linked Data

• dbSNP Id: rs1358750678
• gnomAD v3: 6-31356289-A-G
• gnomAD v4: 6-31356289-A-G
• MyVariant Identifiers: chr6:g.31324066A>G (hg19) ; chr6:g.31356289A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356289A>G , CM000668.2:g.31356289A>G	GRCh38
NC_000006.11:g.31324066A>G , CM000668.1:g.31324066A>G	GRCh37
NC_000006.10:g.31432045A>G	NCBI36
NG_023187.1:g.5924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1970T>C
ENST00000481849.6:n.1970T>C
ENST00000497377.6:n.1970T>C
ENST00000640094.2:c.497T>C	ENSP00000491275.2:p.Ile166Thr
ENST00000696558.1:c.497T>C	ENSP00000512716.1:p.Ile166Thr
ENST00000696559.1:c.497T>C	ENSP00000512717.1:p.Ile166Thr
ENST00000696560.1:c.497T>C	ENSP00000512718.1:p.Ile166Thr
ENST00000696561.1:c.497T>C	ENSP00000512719.1:p.Ile166Thr
ENST00000696562.1:c.497T>C	ENSP00000512720.1:p.Ile166Thr
ENST00000412585.7:c.497T>C MANE Select	ENSP00000399168.2:p.Ile166Thr
ENST00000412585.6:c.497T>C	ENSP00000399168.2:p.Ile166Thr
ENST00000434333.1:c.530T>C	ENSP00000405931.1:p.Ile177Thr
ENST00000474381.1:n.372T>C
ENST00000498007.1:n.763T>C
NM_005514.6:c.497T>C	NP_005505.2:p.Ile166Thr
XM_011514556.1:c.530T>C	XP_011512858.1:p.Ile177Thr
XM_011514557.1:c.497T>C	XP_011512859.1:p.Ile166Thr
XR_926175.1:n.507T>C
NM_005514.7:c.497T>C	NP_005505.2:p.Ile166Thr
NM_005514.8:c.497T>C MANE Select	NP_005505.2:p.Ile166Thr