Canonical Allele Identifier: CA7266384

Gene: VSX2

Linked Data

• dbSNP Id: rs754397036
• ExAC: 14:74726274 C / G
• gnomAD v2: 14-74726274-C-G
• gnomAD v3: 14-74259571-C-G
• gnomAD v4: 14-74259571-C-G
• MyVariant Identifiers: chr14:g.74726274C>G (hg19) ; chr14:g.74259571C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74259571C>G , CM000676.2:g.74259571C>G	GRCh38
NC_000014.8:g.74726274C>G , CM000676.1:g.74726274C>G	GRCh37
NC_000014.7:g.73796027C>G	NCBI36
NG_013092.1:g.25100C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261980.3:c.580-31C>G MANE Select	ENSP00000261980.2:n.580-31C>G
ENST00000261980.2:c.580-31C>G	ENSP00000261980.2:n.580-31C>G
NM_182894.2:c.580-31C>G	NP_878314.1:n.580-31C>G
XM_011536719.1:c.580-31C>G	XP_011535021.1:n.580-31C>G
NM_182894.3:c.580-31C>G MANE Select	NP_878314.1:n.580-31C>G