Canonical Allele Identifier: CA2146964481

Gene: VSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74259669T= , CM000676.2:g.74259669T=	GRCh38
NC_000014.8:g.74726372T= , CM000676.1:g.74726372T=	GRCh37
NC_000014.7:g.73796125T=	NCBI36
NG_013092.1:g.25198T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261980.3:c.647T= MANE Select	ENSP00000261980.2:p.Met216=
ENST00000261980.2:c.647T=	ENSP00000261980.2:p.Met216=
NM_182894.2:c.647T=	NP_878314.1:p.Met216=
XM_011536719.1:c.647T=	XP_011535021.1:p.Met216=
NM_182894.3:c.647T= MANE Select	NP_878314.1:p.Met216=