Canonical Allele Identifier: CA390369068
Gene: VSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1594758748
MyVariant Identifiers: chr14:g.74726318A>C (hg19) chr14:g.74259615A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259615A>C , CM000676.2:g.74259615A>C GRCh38
NC_000014.8:g.74726318A>C , CM000676.1:g.74726318A>C GRCh37
NC_000014.7:g.73796071A>C NCBI36
NG_013092.1:g.25144A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.593A>C MANE Select ENSP00000261980.2:p.Asn198Thr
ENST00000261980.2:c.593A>C ENSP00000261980.2:p.Asn198Thr
NM_182894.2:c.593A>C NP_878314.1:p.Asn198Thr
XM_011536719.1:c.593A>C XP_011535021.1:p.Asn198Thr
NM_182894.3:c.593A>C MANE Select NP_878314.1:p.Asn198Thr
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