Canonical Allele Identifier: CA2146964535
Gene: VSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259790C= , CM000676.2:g.74259790C= GRCh38
NC_000014.8:g.74726493C= , CM000676.1:g.74726493C= GRCh37
NC_000014.7:g.73796246C= NCBI36
NG_013092.1:g.25319C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+8C= MANE Select ENSP00000261980.2:n.760+8C=
ENST00000261980.2:c.760+8C= ENSP00000261980.2:n.760+8C=
NM_182894.2:c.760+8C= NP_878314.1:n.760+8C=
XM_011536719.1:c.760+8C= XP_011535021.1:n.760+8C=
NM_182894.3:c.760+8C= MANE Select NP_878314.1:n.760+8C=