Canonical Allele Identifier: CA2625651025
Gene: VSX2 HGNC NCBI

Linked Data

gnomAD v4: 14-74259534-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259534C>T , CM000676.2:g.74259534C>T GRCh38
NC_000014.8:g.74726237C>T , CM000676.1:g.74726237C>T GRCh37
NC_000014.7:g.73795990C>T NCBI36
NG_013092.1:g.25063C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261980.3:c.580-68C>T MANE Select ENSP00000261980.2:n.580-68C>T
ENST00000261980.2:c.580-68C>T ENSP00000261980.2:n.580-68C>T
NM_182894.2:c.580-68C>T NP_878314.1:n.580-68C>T
XM_011536719.1:c.580-68C>T XP_011535021.1:n.580-68C>T
NM_182894.3:c.580-68C>T MANE Select NP_878314.1:n.580-68C>T
Search 100 bp 5'
Search 100 bp 3'