Canonical Allele Identifier: CA2146964543
Gene: VSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259800C= , CM000676.2:g.74259800C= GRCh38
NC_000014.8:g.74726503C= , CM000676.1:g.74726503C= GRCh37
NC_000014.7:g.73796256C= NCBI36
NG_013092.1:g.25329C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+18C= MANE Select ENSP00000261980.2:n.760+18C=
ENST00000261980.2:c.760+18C= ENSP00000261980.2:n.760+18C=
NM_182894.2:c.760+18C= NP_878314.1:n.760+18C=
XM_011536719.1:c.760+18C= XP_011535021.1:n.760+18C=
NM_182894.3:c.760+18C= MANE Select NP_878314.1:n.760+18C=