Canonical Allele Identifier: CA263556332
Gene: VSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1033606435
MyVariant Identifiers: chr14:g.74726232G>T (hg19) chr14:g.74259529G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259529G>T , CM000676.2:g.74259529G>T GRCh38
NC_000014.8:g.74726232G>T , CM000676.1:g.74726232G>T GRCh37
NC_000014.7:g.73795985G>T NCBI36
NG_013092.1:g.25058G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261980.3:c.580-73G>T MANE Select ENSP00000261980.2:n.580-73G>T
ENST00000261980.2:c.580-73G>T ENSP00000261980.2:n.580-73G>T
NM_182894.2:c.580-73G>T NP_878314.1:n.580-73G>T
XM_011536719.1:c.580-73G>T XP_011535021.1:n.580-73G>T
NM_182894.3:c.580-73G>T MANE Select NP_878314.1:n.580-73G>T
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