Canonical Allele Identifier: CA679208277

Gene: SPINDOC

Linked Data

• dbSNP Id: rs10897449
• MyVariant Identifiers: chr11:g.63592621C>G (hg19) ; chr11:g.63825149C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.63825149C>G , CM000673.2:g.63825149C>G	GRCh38
NC_000011.9:g.63592621C>G , CM000673.1:g.63592621C>G	GRCh37
NC_000011.8:g.63349197C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000294244.9:c.935-1779C>G MANE Select	ENSP00000294244.3:n.935-1779C>G
ENST00000294244.8:c.935-1779C>G	ENSP00000294244.3:n.935-1779C>G
NM_138471.2:c.935-1779C>G	NP_612480.1:n.935-1779C>G
XM_006718437.1:c.993-1779C>G	XP_006718500.1:n.993-1779C>G
XM_011544770.1:c.993-1817C>G	XP_011543072.1:n.993-1817C>G
XM_011544771.1:c.867-1817C>G	XP_011543073.1:n.867-1817C>G
XM_011544772.1:c.935-1817C>G	XP_011543074.1:n.935-1817C>G
XR_001747777.1:n.1466-1779C>G
NM_138471.3:c.935-1779C>G MANE Select	NP_612480.1:n.935-1779C>G