Canonical Allele Identifier: CA136833504

Gene: HLA-B

Linked Data

• dbSNP Id: rs41562214
• gnomAD v3: 6-31356170-C-A
• gnomAD v4: 6-31356170-C-A
• MyVariant Identifiers: chr6:g.31323947C>A (hg19) ; chr6:g.31356170C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356170C>A , CM000668.2:g.31356170C>A	GRCh38
NC_000006.11:g.31323947C>A , CM000668.1:g.31323947C>A	GRCh37
NC_000006.10:g.31431926C>A	NCBI36
NG_023187.1:g.6043G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2089G>T
ENST00000481849.6:n.2089G>T
ENST00000497377.6:n.2089G>T
ENST00000640094.2:c.616G>T	ENSP00000491275.2:p.Ala206Ser
ENST00000696558.1:c.616G>T	ENSP00000512716.1:p.Ala206Ser
ENST00000696559.1:c.616G>T	ENSP00000512717.1:p.Ala206Ser
ENST00000696560.1:c.616G>T	ENSP00000512718.1:p.Ala206Ser
ENST00000696561.1:c.616G>T	ENSP00000512719.1:p.Ala206Ser
ENST00000696562.1:c.616G>T	ENSP00000512720.1:p.Ala206Ser
ENST00000412585.7:c.616G>T MANE Select	ENSP00000399168.2:p.Ala206Ser
ENST00000412585.6:c.616G>T	ENSP00000399168.2:p.Ala206Ser
ENST00000434333.1:c.649G>T	ENSP00000405931.1:p.Ala217Ser
ENST00000474381.1:n.491G>T
ENST00000498007.1:n.882G>T
NM_005514.6:c.616G>T	NP_005505.2:p.Ala206Ser
XM_011514556.1:c.649G>T	XP_011512858.1:p.Ala217Ser
XM_011514557.1:c.616G>T	XP_011512859.1:p.Ala206Ser
XR_926175.1:n.626G>T
NM_005514.7:c.616G>T	NP_005505.2:p.Ala206Ser
NM_005514.8:c.616G>T MANE Select	NP_005505.2:p.Ala206Ser