Canonical Allele Identifier: CA1059273231
Gene: CLNK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10725733T>A , CM000666.2:g.10725733T>A GRCh38
NC_000004.11:g.10727357T>A , CM000666.1:g.10727357T>A GRCh37
NC_000004.10:g.10336455T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011513775.1:c.3+8795A>T XP_011512077.1:n.3+8795A>T
XM_011513775.2:c.3+8795A>T XP_011512077.1:n.3+8795A>T
XM_017007684.1:c.3+8795A>T XP_016863173.1:n.3+8795A>T
XM_017007685.1:c.3+8795A>T XP_016863174.1:n.3+8795A>T