Canonical Allele Identifier: CA390369285
Gene: VSX2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.655T>A MANE Select ENSP00000261980.2:p.Tyr219Asn
ENST00000261980.2:c.655T>A ENSP00000261980.2:p.Tyr219Asn
NM_182894.2:c.655T>A NP_878314.1:p.Tyr219Asn
XM_011536719.1:c.655T>A XP_011535021.1:p.Tyr219Asn
NM_182894.3:c.655T>A MANE Select NP_878314.1:p.Tyr219Asn