Canonical Allele Identifier: CA3710895
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1050409
ExAC: 6:31239501 G / T
gnomAD v2: 6-31239501-G-T
gnomAD v3: 6-31271724-G-T
gnomAD v4: 6-31271724-G-T
MyVariant Identifiers: chr6:g.31239501G>T (hg19) chr6:g.31271724G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271724G>T , CM000668.2:g.31271724G>T GRCh38
NC_000006.11:g.31239501G>T , CM000668.1:g.31239501G>T GRCh37
NC_000006.10:g.31347480G>T NCBI36
NG_029422.2:g.5408C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.218C>A MANE Select ENSP00000365402.5:p.Ala73Glu
ENST00000376228.9:c.218C>A ENSP00000365402.5:p.Ala73Glu
ENST00000376237.8:c.218C>A ENSP00000365412.4:p.Ala73Glu
ENST00000383329.7:c.218C>A ENSP00000372819.3:p.Ala73Glu
ENST00000415537.1:c.216C>A
ENST00000484378.1:n.237C>A
ENST00000487245.5:n.327C>A
ENST00000495835.1:n.407C>A
NM_002117.5:c.218C>A NP_002108.4:p.Ala73Glu
NM_002117.6:c.218C>A MANE Select NP_002108.4:p.Ala73Glu
Search 100 bp 5'
Search 100 bp 3'