Canonical Allele Identifier: CA2677956886

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356420-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356420_31356421insCT , CM000668.2:g.31356420_31356421insCT	GRCh38
NC_000006.11:g.31324197_31324198insCT , CM000668.1:g.31324197_31324198insCT	GRCh37
NC_000006.10:g.31432176_31432177insCT	NCBI36
NG_023187.1:g.5792_5793insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1838_1839insAG
ENST00000481849.6:n.1838_1839insAG
ENST00000497377.6:n.1838_1839insAG
ENST00000640094.2:c.365_366insAG	ENSP00000491275.2:p.Met122IlefsTer30
ENST00000696558.1:c.365_366insAG	ENSP00000512716.1:p.Met122IlefsTer30
ENST00000696559.1:c.365_366insAG	ENSP00000512717.1:p.Met122IlefsTer30
ENST00000696560.1:c.365_366insAG	ENSP00000512718.1:p.Met122IlefsTer30
ENST00000696561.1:c.365_366insAG	ENSP00000512719.1:p.Met122IlefsTer30
ENST00000696562.1:c.365_366insAG	ENSP00000512720.1:p.Met122IlefsTer30
ENST00000412585.7:c.365_366insAG MANE Select	ENSP00000399168.2:p.Met122IlefsTer30
ENST00000412585.6:c.365_366insAG	ENSP00000399168.2:p.Met122IlefsTer30
ENST00000434333.1:c.398_399insAG	ENSP00000405931.1:p.Met133IlefsTer30
ENST00000474381.1:n.240_241insAG
ENST00000498007.1:n.631_632insAG
NM_005514.6:c.365_366insAG	NP_005505.2:p.Met122IlefsTer30
XM_011514556.1:c.398_399insAG	XP_011512858.1:p.Met133IlefsTer30
XM_011514557.1:c.365_366insAG	XP_011512859.1:p.Met122IlefsTer30
XR_926175.1:n.375_376insAG
NM_005514.7:c.365_366insAG	NP_005505.2:p.Met122IlefsTer30
NM_005514.8:c.365_366insAG MANE Select	NP_005505.2:p.Met122IlefsTer30