Canonical Allele Identifier: CA2146964549
Gene: VSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259813C= , CM000676.2:g.74259813C= GRCh38
NC_000014.8:g.74726516C= , CM000676.1:g.74726516C= GRCh37
NC_000014.7:g.73796269C= NCBI36
NG_013092.1:g.25342C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+31C= MANE Select ENSP00000261980.2:n.760+31C=
ENST00000261980.2:c.760+31C= ENSP00000261980.2:n.760+31C=
NM_182894.2:c.760+31C= NP_878314.1:n.760+31C=
XM_011536719.1:c.760+31C= XP_011535021.1:n.760+31C=
NM_182894.3:c.760+31C= MANE Select NP_878314.1:n.760+31C=