Canonical Allele Identifier: CA487155887

Gene: VSX2

Linked Data

• MyVariant Identifiers: chr14:g.74726388C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74259685C>T , CM000676.2:g.74259685C>T	GRCh38
NC_000014.8:g.74726388C>T , CM000676.1:g.74726388C>T	GRCh37
NC_000014.7:g.73796141C>T	NCBI36
NG_013092.1:g.25214C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261980.3:c.663C>T MANE Select	ENSP00000261980.2:p.Leu221=
ENST00000261980.2:c.663C>T	ENSP00000261980.2:p.Leu221=
NM_182894.2:c.663C>T	NP_878314.1:p.Leu221=
XM_011536719.1:c.663C>T	XP_011535021.1:p.Leu221=
NM_182894.3:c.663C>T MANE Select	NP_878314.1:p.Leu221=