Canonical Allele Identifier: CA1438225272
Gene: CLNK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10725229C= , CM000666.2:g.10725229C= GRCh38
NC_000004.11:g.10726853C= , CM000666.1:g.10726853C= GRCh37
NC_000004.10:g.10335951C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011513775.1:c.3+9299G= XP_011512077.1:n.3+9299G=
XM_011513775.2:c.3+9299G= XP_011512077.1:n.3+9299G=
XM_017007684.1:c.3+9299G= XP_016863173.1:n.3+9299G=
XM_017007685.1:c.3+9299G= XP_016863174.1:n.3+9299G=