Canonical Allele Identifier: CA2625651088
Gene: VSX2 HGNC NCBI

Linked Data

gnomAD v4: 14-74259839-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259841del , CM000676.2:g.74259841del GRCh38
NC_000014.8:g.74726544del , CM000676.1:g.74726544del GRCh37
NC_000014.7:g.73796297del NCBI36
NG_013092.1:g.25370del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+59del MANE Select ENSP00000261980.2:n.760+59del
ENST00000261980.2:c.760+59del ENSP00000261980.2:n.760+59del
NM_182894.2:c.760+59del NP_878314.1:n.760+59del
XM_011536719.1:c.760+59del XP_011535021.1:n.760+59del
NM_182894.3:c.760+59del MANE Select NP_878314.1:n.760+59del
Search 100 bp 5'
Search 100 bp 3'