Canonical Allele Identifier: CA487155839
Gene: VSX2 HGNC NCBI

Linked Data

gnomAD v4: 14-74259643-G-A
MyVariant Identifiers: chr14:g.74726346G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259643G>A , CM000676.2:g.74259643G>A GRCh38
NC_000014.8:g.74726346G>A , CM000676.1:g.74726346G>A GRCh37
NC_000014.7:g.73796099G>A NCBI36
NG_013092.1:g.25172G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.621G>A MANE Select ENSP00000261980.2:p.Glu207=
ENST00000261980.2:c.621G>A ENSP00000261980.2:p.Glu207=
NM_182894.2:c.621G>A NP_878314.1:p.Glu207=
XM_011536719.1:c.621G>A XP_011535021.1:p.Glu207=
NM_182894.3:c.621G>A MANE Select NP_878314.1:p.Glu207=
Search 100 bp 5'
Search 100 bp 3'