Canonical Allele Identifier: CA449790848

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357168-T-G
• MyVariant Identifiers: chr6:g.31324945T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357168T>G , CM000668.2:g.31357168T>G	GRCh38
NC_000006.11:g.31324945T>G , CM000668.1:g.31324945T>G	GRCh37
NC_000006.10:g.31432924T>G	NCBI36
NG_023187.1:g.5045A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1464A>C
ENST00000481849.6:n.1464A>C
ENST00000497377.6:n.1464A>C
ENST00000696559.1:c.-10A>C	ENSP00000512717.1:n.-10A>C
ENST00000696560.1:c.-10A>C	ENSP00000512718.1:n.-10A>C
ENST00000696561.1:c.-10A>C	ENSP00000512719.1:n.-10A>C
ENST00000696562.1:c.-10A>C	ENSP00000512720.1:n.-10A>C
ENST00000412585.7:c.-10A>C MANE Select	ENSP00000399168.2:n.-10A>C
ENST00000412585.6:c.-10A>C	ENSP00000399168.2:n.-10A>C
ENST00000434333.1:c.-105A>C	ENSP00000405931.1:n.-105A>C
ENST00000498007.1:n.12A>C
ENST00000603274.1:n.522T>G
NM_005514.6:c.-10A>C	NP_005505.2:n.-10A>C
XM_011514557.1:c.-10A>C	XP_011512859.1:n.-10A>C
XR_926175.1:n.1A>C
NM_005514.7:c.-10A>C	NP_005505.2:n.-10A>C
NM_005514.8:c.-10A>C MANE Select	NP_005505.2:n.-10A>C