Canonical Allele Identifier: CA449790429
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs200892438
gnomAD v2: 6-31238986-G-A
gnomAD v3: 6-31271209-G-A
gnomAD v4: 6-31271209-G-A
MyVariant Identifiers: chr6:g.31238986G>A (hg19) chr6:g.31271209G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271209G>A , CM000668.2:g.31271209G>A GRCh38
NC_000006.11:g.31238986G>A , CM000668.1:g.31238986G>A GRCh37
NC_000006.10:g.31346965G>A NCBI36
NG_029422.2:g.5923C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.483C>T MANE Select ENSP00000365402.5:p.Asp161=
ENST00000376228.9:c.483C>T ENSP00000365402.5:p.Asp161=
ENST00000376237.8:c.*70C>T ENSP00000365412.4:n.*70C>T
ENST00000383329.7:c.483C>T ENSP00000372819.3:p.Asp161=
ENST00000415537.1:c.481C>T
ENST00000484378.1:n.752C>T
ENST00000487245.5:n.842C>T
ENST00000495835.1:n.672C>T
NM_002117.5:c.483C>T NP_002108.4:p.Asp161=
NM_002117.6:c.483C>T MANE Select NP_002108.4:p.Asp161=
Search 100 bp 5'
Search 100 bp 3'