Canonical Allele Identifier: CA412974421
Gene: XK HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37587158G>C (hg19) chrX:g.37727905G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727905G>C , CM000685.2:g.37727905G>C GRCh38
NC_000023.10:g.37587158G>C , CM000685.1:g.37587158G>C GRCh37
NC_000023.9:g.37472097G>C NCBI36
NG_007473.1:g.47046G>C
NG_007473.3:g.47026G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.778G>C MANE Select ENSP00000367879.3:p.Gly260Arg
ENST00000378616.3:c.778G>C ENSP00000367879.3:p.Gly260Arg
ENST00000465127.1:c.171+301905G>C ENSP00000417050.1:n.171+301905G>C
NM_021083.2:c.778G>C NP_066569.1:p.Gly260Arg
NM_021083.4:c.778G>C MANE Select NP_066569.1:p.Gly260Arg
Search 100 bp 5'
Search 100 bp 3'