Canonical Allele Identifier: CA487155809
Gene: VSX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.74726316G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259613G>A , CM000676.2:g.74259613G>A GRCh38
NC_000014.8:g.74726316G>A , CM000676.1:g.74726316G>A GRCh37
NC_000014.7:g.73796069G>A NCBI36
NG_013092.1:g.25142G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.591G>A MANE Select ENSP00000261980.2:p.Gln197=
ENST00000261980.2:c.591G>A ENSP00000261980.2:p.Gln197=
NM_182894.2:c.591G>A NP_878314.1:p.Gln197=
XM_011536719.1:c.591G>A XP_011535021.1:p.Gln197=
NM_182894.3:c.591G>A MANE Select NP_878314.1:p.Gln197=
Search 100 bp 5'
Search 100 bp 3'