Canonical Allele Identifier: CA363314668

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31357038-C-G
• gnomAD v4: 6-31357038-C-G
• MyVariant Identifiers: chr6:g.31324815C>G (hg19) ; chr6:g.31357038C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357038C>G , CM000668.2:g.31357038C>G	GRCh38
NC_000006.11:g.31324815C>G , CM000668.1:g.31324815C>G	GRCh37
NC_000006.10:g.31432794C>G	NCBI36
NG_023187.1:g.5175G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1546+48G>C
ENST00000481849.6:n.1546+48G>C
ENST00000497377.6:n.1546+48G>C
ENST00000640094.2:c.73+48G>C	ENSP00000491275.2:n.73+48G>C
ENST00000696558.1:c.73+48G>C	ENSP00000512716.1:n.73+48G>C
ENST00000696559.1:c.73+48G>C	ENSP00000512717.1:n.73+48G>C
ENST00000696560.1:c.73+48G>C	ENSP00000512718.1:n.73+48G>C
ENST00000696561.1:c.73+48G>C	ENSP00000512719.1:n.73+48G>C
ENST00000696562.1:c.73+48G>C	ENSP00000512720.1:n.73+48G>C
ENST00000412585.7:c.73+48G>C MANE Select	ENSP00000399168.2:n.73+48G>C
ENST00000412585.6:c.73+48G>C	ENSP00000399168.2:n.73+48G>C
ENST00000434333.1:c.26G>C	ENSP00000405931.1:p.Gly9Ala
ENST00000498007.1:n.94+48G>C
ENST00000603274.1:n.392C>G
NM_005514.6:c.73+48G>C	NP_005505.2:n.73+48G>C
XM_011514556.1:c.26G>C	XP_011512858.1:p.Gly9Ala
XM_011514557.1:c.73+48G>C	XP_011512859.1:n.73+48G>C
XR_926175.1:n.83+48G>C
NM_005514.7:c.73+48G>C	NP_005505.2:n.73+48G>C
NM_005514.8:c.73+48G>C MANE Select	NP_005505.2:n.73+48G>C