Canonical Allele Identifier: CA2625651032
Gene: VSX2 HGNC NCBI

Linked Data

gnomAD v4: 14-74259550-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259550T>G , CM000676.2:g.74259550T>G GRCh38
NC_000014.8:g.74726253T>G , CM000676.1:g.74726253T>G GRCh37
NC_000014.7:g.73796006T>G NCBI36
NG_013092.1:g.25079T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261980.3:c.580-52T>G MANE Select ENSP00000261980.2:n.580-52T>G
ENST00000261980.2:c.580-52T>G ENSP00000261980.2:n.580-52T>G
NM_182894.2:c.580-52T>G NP_878314.1:n.580-52T>G
XM_011536719.1:c.580-52T>G XP_011535021.1:n.580-52T>G
NM_182894.3:c.580-52T>G MANE Select NP_878314.1:n.580-52T>G
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