Canonical Allele Identifier: CA2146964536
Gene: VSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259792C= , CM000676.2:g.74259792C= GRCh38
NC_000014.8:g.74726495C= , CM000676.1:g.74726495C= GRCh37
NC_000014.7:g.73796248C= NCBI36
NG_013092.1:g.25321C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+10C= MANE Select ENSP00000261980.2:n.760+10C=
ENST00000261980.2:c.760+10C= ENSP00000261980.2:n.760+10C=
NM_182894.2:c.760+10C= NP_878314.1:n.760+10C=
XM_011536719.1:c.760+10C= XP_011535021.1:n.760+10C=
NM_182894.3:c.760+10C= MANE Select NP_878314.1:n.760+10C=