Canonical Allele Identifier: CA12187580

Gene: HLA-B

Linked Data

• dbSNP Id: rs2768
• gnomAD v2: 6-31321856-A-G
• gnomAD v3: 6-31354079-A-G
• gnomAD v4: 6-31354079-A-G
• MyVariant Identifiers: chr6:g.31321856A>G (hg19) ; chr6:g.31354079A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354079A>G , CM000668.2:g.31354079A>G	GRCh38
NC_000006.11:g.31321856A>G , CM000668.1:g.31321856A>G	GRCh37
NC_000006.10:g.31429835A>G	NCBI36
NG_023187.1:g.8134T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3358T>C
ENST00000481849.6:n.3318T>C
ENST00000497377.6:n.3225T>C
ENST00000696558.1:c.1380T>C	ENSP00000512716.1:n.1380T>C
ENST00000696559.1:c.*222T>C	ENSP00000512717.1:n.*222T>C
ENST00000696560.1:c.*222T>C	ENSP00000512718.1:n.*222T>C
ENST00000696561.1:c.*222T>C	ENSP00000512719.1:n.*222T>C
ENST00000696562.1:c.*222T>C	ENSP00000512720.1:n.*222T>C
ENST00000412585.7:c.*222T>C MANE Select	ENSP00000399168.2:n.*222T>C
ENST00000412585.6:c.*222T>C	ENSP00000399168.2:n.*222T>C
ENST00000481849.5:n.546T>C
ENST00000497377.5:n.710T>C
NM_005514.6:c.*222T>C	NP_005505.2:n.*222T>C
XM_011514556.1:c.*222T>C	XP_011512858.1:n.*222T>C
XM_011514557.1:c.*222T>C	XP_011512859.1:n.*222T>C
XR_926175.1:n.1750T>C
NM_005514.7:c.*222T>C	NP_005505.2:n.*222T>C
NM_005514.8:c.*222T>C MANE Select	NP_005505.2:n.*222T>C