Canonical Allele Identifier: CA12713624
Gene: XKR6 HGNC NCBI

Linked Data

dbSNP Id: rs6982751
gnomAD v2: 8-10813474-C-G
gnomAD v3: 8-10955964-C-G
gnomAD v4: 8-10955964-C-G

Genomic Alleles

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

Transcript Alleles

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