Canonical Allele Identifier: CA565893363
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs1368990649
gnomAD v2: 6-29909717-GTC-G
gnomAD v3: 6-29941940-GTC-G
gnomAD v4: 6-29941940-GTC-G
MyVariant Identifiers: chr6:g.29909718_29909719del (hg19) chr6:g.29941941_29941942del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29941944_29941945del , CM000668.2:g.29941944_29941945del GRCh38
NC_000006.11:g.29909721_29909722del , CM000668.1:g.29909721_29909722del GRCh37
NC_000006.10:g.30017700_30017701del NCBI36
NG_029217.2:g.4482_4483del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396634.5:c.-281-22_-281-21del ENSP00000379873.1:n.-281-22_-281-21del
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