Canonical Allele Identifier: CA487155976

Gene: VSX2

Linked Data

• dbSNP Id: rs2079291600
• MyVariant Identifiers: chr14:g.74726463C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74259760C>T , CM000676.2:g.74259760C>T	GRCh38
NC_000014.8:g.74726463C>T , CM000676.1:g.74726463C>T	GRCh37
NC_000014.7:g.73796216C>T	NCBI36
NG_013092.1:g.25289C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261980.3:c.738C>T MANE Select	ENSP00000261980.2:p.Asp246=
ENST00000261980.2:c.738C>T	ENSP00000261980.2:p.Asp246=
NM_182894.2:c.738C>T	NP_878314.1:p.Asp246=
XM_011536719.1:c.738C>T	XP_011535021.1:p.Asp246=
NM_182894.3:c.738C>T MANE Select	NP_878314.1:p.Asp246=