Canonical Allele Identifier: CA390369287
Gene: VSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1594758784

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259677T>G , CM000676.2:g.74259677T>G GRCh38
NC_000014.8:g.74726380T>G , CM000676.1:g.74726380T>G GRCh37
NC_000014.7:g.73796133T>G NCBI36
NG_013092.1:g.25206T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.655T>G MANE Select ENSP00000261980.2:p.Tyr219Asp
ENST00000261980.2:c.655T>G ENSP00000261980.2:p.Tyr219Asp
NM_182894.2:c.655T>G NP_878314.1:p.Tyr219Asp
XM_011536719.1:c.655T>G XP_011535021.1:p.Tyr219Asp
NM_182894.3:c.655T>G MANE Select NP_878314.1:p.Tyr219Asp