Canonical Allele Identifier: CA2146964429
Gene: VSX2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259553G= , CM000676.2:g.74259553G= GRCh38
NC_000014.8:g.74726256G= , CM000676.1:g.74726256G= GRCh37
NC_000014.7:g.73796009G= NCBI36
NG_013092.1:g.25082G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261980.3:c.580-49G= MANE Select ENSP00000261980.2:n.580-49G=
ENST00000261980.2:c.580-49G= ENSP00000261980.2:n.580-49G=
NM_182894.2:c.580-49G= NP_878314.1:n.580-49G=
XM_011536719.1:c.580-49G= XP_011535021.1:n.580-49G=
NM_182894.3:c.580-49G= MANE Select NP_878314.1:n.580-49G=
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