Canonical Allele Identifier: CA11772017

Gene: CLNK

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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