Canonical Allele Identifier: CA390369483
Gene: VSX2 HGNC NCBI

Linked Data

gnomAD v4: 14-74259768-C-G
MyVariant Identifiers: chr14:g.74726471C>G (hg19) chr14:g.74259768C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259768C>G , CM000676.2:g.74259768C>G GRCh38
NC_000014.8:g.74726471C>G , CM000676.1:g.74726471C>G GRCh37
NC_000014.7:g.73796224C>G NCBI36
NG_013092.1:g.25297C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.746C>G MANE Select ENSP00000261980.2:p.Ala249Gly
ENST00000261980.2:c.746C>G ENSP00000261980.2:p.Ala249Gly
NM_182894.2:c.746C>G NP_878314.1:p.Ala249Gly
XM_011536719.1:c.746C>G XP_011535021.1:p.Ala249Gly
NM_182894.3:c.746C>G MANE Select NP_878314.1:p.Ala249Gly
Search 100 bp 5'
Search 100 bp 3'