Canonical Allele Identifier: CA580011039
Gene: XKR6 HGNC NCBI

Linked Data

dbSNP Id: rs6982751
gnomAD v2: 8-10813474-C-T
gnomAD v3: 8-10955964-C-T
gnomAD v4: 8-10955964-C-T
MyVariant Identifiers: chr8:g.10813474C>T (hg19) chr8:g.10955964C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10955964C>T , CM000670.2:g.10955964C>T GRCh38
NC_000008.10:g.10813474C>T , CM000670.1:g.10813474C>T GRCh37
NC_000008.9:g.10850884C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000382461.8:c.-13-31134G>A ENSP00000371900.4:n.-13-31134G>A
ENST00000416569.3:c.765-31134G>A MANE Select ENSP00000416707.2:n.765-31134G>A
ENST00000382461.7:c.95-31134G>A
ENST00000416569.2:c.765-31134G>A ENSP00000416707.2:n.765-31134G>A
NM_173683.3:c.765-31134G>A NP_775954.2:n.765-31134G>A
XM_024447129.1:c.765-31134G>A XP_024302897.1:n.765-31134G>A
NM_173683.4:c.765-31134G>A MANE Select NP_775954.2:n.765-31134G>A
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