Canonical Allele Identifier: CA615033748
Gene: VSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1367343566
gnomAD v2: 14-74726254-G-A
gnomAD v4: 14-74259551-G-A
MyVariant Identifiers: chr14:g.74726254G>A (hg19) chr14:g.74259551G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259551G>A , CM000676.2:g.74259551G>A GRCh38
NC_000014.8:g.74726254G>A , CM000676.1:g.74726254G>A GRCh37
NC_000014.7:g.73796007G>A NCBI36
NG_013092.1:g.25080G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261980.3:c.580-51G>A MANE Select ENSP00000261980.2:n.580-51G>A
ENST00000261980.2:c.580-51G>A ENSP00000261980.2:n.580-51G>A
NM_182894.2:c.580-51G>A NP_878314.1:n.580-51G>A
XM_011536719.1:c.580-51G>A XP_011535021.1:n.580-51G>A
NM_182894.3:c.580-51G>A MANE Select NP_878314.1:n.580-51G>A
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