Canonical Allele Identifier: CA1306193763
Gene: SPC25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168900844C= , CM000664.2:g.168900844C= GRCh38
NC_000002.11:g.169757354C= , CM000664.1:g.169757354C= GRCh37
NC_000002.10:g.169465600C= NCBI36
NG_011682.1:g.4605C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000451987.5:c.-172-10158G= ENSP00000393322.1:n.-172-10158G=
ENST00000472216.2:n.177-10158G=