Canonical Allele Identifier: CA487155852
Gene: VSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1033207603
MyVariant Identifiers: chr14:g.74726359C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259656C>A , CM000676.2:g.74259656C>A GRCh38
NC_000014.8:g.74726359C>A , CM000676.1:g.74726359C>A GRCh37
NC_000014.7:g.73796112C>A NCBI36
NG_013092.1:g.25185C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.634C>A MANE Select ENSP00000261980.2:p.Arg212=
ENST00000261980.2:c.634C>A ENSP00000261980.2:p.Arg212=
NM_182894.2:c.634C>A NP_878314.1:p.Arg212=
XM_011536719.1:c.634C>A XP_011535021.1:p.Arg212=
NM_182894.3:c.634C>A MANE Select NP_878314.1:p.Arg212=
Search 100 bp 5'
Search 100 bp 3'