Canonical Allele Identifier: CA390369490
Gene: VSX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.74726476T>C (hg19) chr14:g.74259773T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259773T>C , CM000676.2:g.74259773T>C GRCh38
NC_000014.8:g.74726476T>C , CM000676.1:g.74726476T>C GRCh37
NC_000014.7:g.73796229T>C NCBI36
NG_013092.1:g.25302T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.751T>C MANE Select ENSP00000261980.2:p.Trp251Arg
ENST00000261980.2:c.751T>C ENSP00000261980.2:p.Trp251Arg
NM_182894.2:c.751T>C NP_878314.1:p.Trp251Arg
XM_011536719.1:c.751T>C XP_011535021.1:p.Trp251Arg
NM_182894.3:c.751T>C MANE Select NP_878314.1:p.Trp251Arg
Search 100 bp 5'
Search 100 bp 3'