Canonical Allele Identifier: CA823883934

Gene: HLA-B

Linked Data

• dbSNP Id: rs1467112267
• MyVariant Identifiers: chr6:g.31327101G>T (hg19) ; chr6:g.31359324G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31359324G>T , CM000668.2:g.31359324G>T	GRCh38
NC_000006.11:g.31327101G>T , CM000668.1:g.31327101G>T	GRCh37
NC_000006.10:g.31435080G>T	NCBI36
NG_023187.1:g.2889C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1271-1643C>A
ENST00000481849.6:n.1271-1643C>A
ENST00000497377.6:n.1271-1643C>A
ENST00000696559.1:c.-203-1643C>A	ENSP00000512717.1:n.-203-1643C>A
ENST00000696560.1:c.-203-1643C>A	ENSP00000512718.1:n.-203-1643C>A
ENST00000696561.1:c.-203-1643C>A	ENSP00000512719.1:n.-203-1643C>A
ENST00000696562.1:c.-135-2031C>A	ENSP00000512720.1:n.-135-2031C>A