Canonical Allele Identifier: CA449601355

Gene: HLA-B

Linked Data

• dbSNP Id: rs1130992
• gnomAD v3: 6-31355219-C-G
• gnomAD v4: 6-31355219-C-G
• MyVariant Identifiers: chr6:g.31322996C>G (hg19) ; chr6:g.31355219C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355219C>G , CM000668.2:g.31355219C>G	GRCh38
NC_000006.11:g.31322996C>G , CM000668.1:g.31322996C>G	GRCh37
NC_000006.10:g.31430975C>G	NCBI36
NG_023187.1:g.6994G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2947G>C
ENST00000481849.6:n.2466G>C
ENST00000497377.6:n.2373G>C
ENST00000640094.2:c.895+98G>C	ENSP00000491275.2:n.895+98G>C
ENST00000696558.1:c.969G>C	ENSP00000512716.1:n.969G>C
ENST00000696559.1:c.900G>C	ENSP00000512717.1:p.Pro300=
ENST00000696560.1:c.900G>C	ENSP00000512718.1:p.Pro300=
ENST00000696561.1:c.900G>C	ENSP00000512719.1:p.Pro300=
ENST00000696562.1:c.900G>C	ENSP00000512720.1:p.Pro300=
ENST00000412585.7:c.900G>C MANE Select	ENSP00000399168.2:p.Pro300=
ENST00000640094.1:c.88+98G>C	ENSP00000491275.1:n.88+98G>C
ENST00000412585.6:c.900G>C	ENSP00000399168.2:p.Pro300=
ENST00000463574.1:n.491G>C
NM_005514.6:c.900G>C	NP_005505.2:p.Pro300=
XM_011514556.1:c.933G>C	XP_011512858.1:p.Pro311=
XM_011514557.1:c.895+98G>C	XP_011512859.1:n.895+98G>C
XR_926175.1:n.1339G>C
NM_005514.7:c.900G>C	NP_005505.2:p.Pro300=
NM_005514.8:c.900G>C MANE Select	NP_005505.2:p.Pro300=