Canonical Allele Identifier: CA390369445
Gene: VSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259752A>G , CM000676.2:g.74259752A>G GRCh38
NC_000014.8:g.74726455A>G , CM000676.1:g.74726455A>G GRCh37
NC_000014.7:g.73796208A>G NCBI36
NG_013092.1:g.25281A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.730A>G MANE Select ENSP00000261980.2:p.Ile244Val
ENST00000261980.2:c.730A>G ENSP00000261980.2:p.Ile244Val
NM_182894.2:c.730A>G NP_878314.1:p.Ile244Val
XM_011536719.1:c.730A>G XP_011535021.1:p.Ile244Val
NM_182894.3:c.730A>G MANE Select NP_878314.1:p.Ile244Val