Canonical Allele Identifier: CA136836598

Gene: HLA-B

Linked Data

• dbSNP Id: rs41552516
• gnomAD v2: 6-31324617-G-A
• gnomAD v4: 6-31356840-G-A
• MyVariant Identifiers: chr6:g.31324617G>A (hg19) ; chr6:g.31356840G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356840G>A , CM000668.2:g.31356840G>A	GRCh38
NC_000006.11:g.31324617G>A , CM000668.1:g.31324617G>A	GRCh37
NC_000006.10:g.31432596G>A	NCBI36
NG_023187.1:g.5373C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1664C>T
ENST00000481849.6:n.1664C>T
ENST00000497377.6:n.1664C>T
ENST00000640094.2:c.191C>T	ENSP00000491275.2:p.Ala64Val
ENST00000696558.1:c.191C>T	ENSP00000512716.1:p.Ala64Val
ENST00000696559.1:c.191C>T	ENSP00000512717.1:p.Ala64Val
ENST00000696560.1:c.191C>T	ENSP00000512718.1:p.Ala64Val
ENST00000696561.1:c.191C>T	ENSP00000512719.1:p.Ala64Val
ENST00000696562.1:c.191C>T	ENSP00000512720.1:p.Ala64Val
ENST00000412585.7:c.191C>T MANE Select	ENSP00000399168.2:p.Ala64Val
ENST00000412585.6:c.191C>T	ENSP00000399168.2:p.Ala64Val
ENST00000434333.1:c.224C>T	ENSP00000405931.1:p.Ala75Val
ENST00000474381.1:n.66C>T
ENST00000498007.1:n.212C>T
ENST00000603274.1:n.194G>A
NM_005514.6:c.191C>T	NP_005505.2:p.Ala64Val
XM_011514556.1:c.224C>T	XP_011512858.1:p.Ala75Val
XM_011514557.1:c.191C>T	XP_011512859.1:p.Ala64Val
XR_926175.1:n.201C>T
NM_005514.7:c.191C>T	NP_005505.2:p.Ala64Val
NM_005514.8:c.191C>T MANE Select	NP_005505.2:p.Ala64Val