Canonical Allele Identifier: CA390369420
Gene: VSX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.74726444C>A (hg19) chr14:g.74259741C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259741C>A , CM000676.2:g.74259741C>A GRCh38
NC_000014.8:g.74726444C>A , CM000676.1:g.74726444C>A GRCh37
NC_000014.7:g.73796197C>A NCBI36
NG_013092.1:g.25270C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.719C>A MANE Select ENSP00000261980.2:p.Ala240Asp
ENST00000261980.2:c.719C>A ENSP00000261980.2:p.Ala240Asp
NM_182894.2:c.719C>A NP_878314.1:p.Ala240Asp
XM_011536719.1:c.719C>A XP_011535021.1:p.Ala240Asp
NM_182894.3:c.719C>A MANE Select NP_878314.1:p.Ala240Asp
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