Canonical Allele Identifier: CA2146964490

Gene: VSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74259686T= , CM000676.2:g.74259686T=	GRCh38
NC_000014.8:g.74726389T= , CM000676.1:g.74726389T=	GRCh37
NC_000014.7:g.73796142T=	NCBI36
NG_013092.1:g.25215T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261980.3:c.664T= MANE Select	ENSP00000261980.2:p.Tyr222=
ENST00000261980.2:c.664T=	ENSP00000261980.2:p.Tyr222=
NM_182894.2:c.664T=	NP_878314.1:p.Tyr222=
XM_011536719.1:c.664T=	XP_011535021.1:p.Tyr222=
NM_182894.3:c.664T= MANE Select	NP_878314.1:p.Tyr222=