Canonical Allele Identifier: CA263556600
Gene: VSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1037936559
gnomAD v4: 14-74259709-C-T
MyVariant Identifiers: chr14:g.74726412C>T (hg19) chr14:g.74259709C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259709C>T , CM000676.2:g.74259709C>T GRCh38
NC_000014.8:g.74726412C>T , CM000676.1:g.74726412C>T GRCh37
NC_000014.7:g.73796165C>T NCBI36
NG_013092.1:g.25238C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.687C>T MANE Select ENSP00000261980.2:p.Ser229=
ENST00000261980.2:c.687C>T ENSP00000261980.2:p.Ser229=
NM_182894.2:c.687C>T NP_878314.1:p.Ser229=
XM_011536719.1:c.687C>T XP_011535021.1:p.Ser229=
NM_182894.3:c.687C>T MANE Select NP_878314.1:p.Ser229=
Search 100 bp 5'
Search 100 bp 3'