Canonical Allele Identifier: CA136024407
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs199474604
gnomAD v4: 6-29943979-C-T
MyVariant Identifiers: chr6:g.29911756C>T (hg19) chr6:g.29943979C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943979C>T , CM000668.2:g.29943979C>T GRCh38
NC_000006.11:g.29911756C>T , CM000668.1:g.29911756C>T GRCh37
NC_000006.10:g.30019735C>T NCBI36
NG_029217.2:g.6515C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.620-143C>T ENSP00000492789.2:n.620-143C>T
ENST00000706892.1:n.1331C>T
ENST00000706893.1:c.620-143C>T ENSP00000516609.1:n.620-143C>T
ENST00000706894.1:c.620-143C>T ENSP00000516610.1:n.620-143C>T
ENST00000706895.1:n.896-143C>T
ENST00000706896.1:n.1331C>T
ENST00000706897.1:n.896-143C>T
ENST00000706898.1:c.620-143C>T ENSP00000516611.1:n.620-143C>T
ENST00000706899.1:n.1331C>T
ENST00000706900.1:c.536-143C>T ENSP00000516617.1:n.536-143C>T
ENST00000706901.1:c.620-143C>T ENSP00000516612.1:n.620-143C>T
ENST00000706902.1:c.620-143C>T ENSP00000516613.1:n.620-143C>T
ENST00000706903.1:c.620-143C>T ENSP00000516614.1:n.620-143C>T
ENST00000706904.1:c.620-143C>T ENSP00000516615.1:n.620-143C>T
ENST00000706905.1:c.620-143C>T ENSP00000516616.1:n.620-143C>T
ENST00000376809.10:c.620-143C>T MANE Select ENSP00000366005.5:n.620-143C>T
ENST00000638375.1:c.620-143C>T ENSP00000492789.1:n.620-143C>T
ENST00000376802.2:c.620-143C>T ENSP00000365998.2:n.620-143C>T
ENST00000376806.9:c.620-143C>T ENSP00000366002.5:n.620-143C>T
ENST00000376809.9:c.620-143C>T ENSP00000366005.5:n.620-143C>T
ENST00000396634.5:c.620-143C>T ENSP00000379873.1:n.620-143C>T
ENST00000461903.1:n.861-143C>T
ENST00000479320.5:n.861-143C>T
ENST00000495183.5:n.863-143C>T
ENST00000496081.5:n.437-143C>T
NM_002116.7:c.620-143C>T NP_002107.3:n.620-143C>T
NM_002116.8:c.620-143C>T MANE Select NP_002107.3:n.620-143C>T
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