Canonical Allele Identifier: CA487155928
Gene: VSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1296317098
gnomAD v2: 14-74726419-C-T
gnomAD v4: 14-74259716-C-T
MyVariant Identifiers: chr14:g.74726419C>T (hg19) chr14:g.74259716C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259716C>T , CM000676.2:g.74259716C>T GRCh38
NC_000014.8:g.74726419C>T , CM000676.1:g.74726419C>T GRCh37
NC_000014.7:g.73796172C>T NCBI36
NG_013092.1:g.25245C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.694C>T MANE Select ENSP00000261980.2:p.Leu232=
ENST00000261980.2:c.694C>T ENSP00000261980.2:p.Leu232=
NM_182894.2:c.694C>T NP_878314.1:p.Leu232=
XM_011536719.1:c.694C>T XP_011535021.1:p.Leu232=
NM_182894.3:c.694C>T MANE Select NP_878314.1:p.Leu232=
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Search 100 bp 3'