Canonical Allele Identifier: CA2146964512

Gene: VSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74259731C= , CM000676.2:g.74259731C=	GRCh38
NC_000014.8:g.74726434C= , CM000676.1:g.74726434C=	GRCh37
NC_000014.7:g.73796187C=	NCBI36
NG_013092.1:g.25260C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261980.3:c.709C= MANE Select	ENSP00000261980.2:p.Leu237=
ENST00000261980.2:c.709C=	ENSP00000261980.2:p.Leu237=
NM_182894.2:c.709C=	NP_878314.1:p.Leu237=
XM_011536719.1:c.709C=	XP_011535021.1:p.Leu237=
NM_182894.3:c.709C= MANE Select	NP_878314.1:p.Leu237=