Canonical Allele Identifier: CA566340054

Gene: HLA-B

Linked Data

• dbSNP Id: rs1562159451
• gnomAD v2: 6-31321806-C-CCAT
• gnomAD v3: 6-31354029-C-CCAT
• gnomAD v4: 6-31354029-C-CCAT
• MyVariant Identifiers: chr6:g.31321806_31321807insCAT (hg19) ; chr6:g.31354029_31354030insCAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354029_31354030insCAT , CM000668.2:g.31354029_31354030insCAT	GRCh38
NC_000006.11:g.31321806_31321807insCAT , CM000668.1:g.31321806_31321807insCAT	GRCh37
NC_000006.10:g.31429785_31429786insCAT	NCBI36
NG_023187.1:g.8183_8184insATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3407_3408insATG
ENST00000481849.6:n.3367_3368insATG
ENST00000497377.6:n.3274_3275insATG
ENST00000696558.1:c.1429_1430insATG	ENSP00000512716.1:n.1429_1430insATG
ENST00000696559.1:c.*271_*272insATG	ENSP00000512717.1:n.*271_*272insATG
ENST00000696560.1:c.*271_*272insATG	ENSP00000512718.1:n.*271_*272insATG
ENST00000696561.1:c.*271_*272insATG	ENSP00000512719.1:n.*271_*272insATG
ENST00000696562.1:c.*271_*272insATG	ENSP00000512720.1:n.*271_*272insATG
ENST00000412585.7:c.*271_*272insATG MANE Select	ENSP00000399168.2:n.*271_*272insATG
ENST00000412585.6:c.*271_*272insATG	ENSP00000399168.2:n.*271_*272insATG
ENST00000481849.5:n.595_596insATG
ENST00000497377.5:n.759_760insATG
NM_005514.6:c.*271_*272insATG	NP_005505.2:n.*271_*272insATG
XM_011514556.1:c.*271_*272insATG	XP_011512858.1:n.*271_*272insATG
XM_011514557.1:c.*271_*272insATG	XP_011512859.1:n.*271_*272insATG
XR_926175.1:n.1799_1800insATG
NM_005514.7:c.*271_*272insATG	NP_005505.2:n.*271_*272insATG
NM_005514.8:c.*271_*272insATG MANE Select	NP_005505.2:n.*271_*272insATG