Canonical Allele Identifier: CA487155995
Gene: VSX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.74726484G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259781G>C , CM000676.2:g.74259781G>C GRCh38
NC_000014.8:g.74726484G>C , CM000676.1:g.74726484G>C GRCh37
NC_000014.7:g.73796237G>C NCBI36
NG_013092.1:g.25310G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.759G>C MANE Select ENSP00000261980.2:p.Leu253=
ENST00000261980.2:c.759G>C ENSP00000261980.2:p.Leu253=
NM_182894.2:c.759G>C NP_878314.1:p.Leu253=
XM_011536719.1:c.759G>C XP_011535021.1:p.Leu253=
NM_182894.3:c.759G>C MANE Select NP_878314.1:p.Leu253=
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